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Jeffrey A Brinker, M.D.

Jeffrey A Brinker, M.D.

  • Professor of Medicine
  • Joint Appointment in Radiology and Radiological Science

https://www.hopkinsmedicine.org/profiles/results/directory/profile/0001297/jeffrey-brinker

These may be purchase 40 mg simvastatin amex cholesterol jumped 50 points, but are not limited to Enlarged Aortic Root 40mg simvastatin cholesterol cell membrane, Small Left Atrium best simvastatin 10mg cholesterol in eggs vs beef, Marked Right Atrial Enlargement, Marked Distortion of the Thorax Configuration. Kyphosis or Scoliosis Potential Adverse Events Adverse events may vary in severity and may require medical or surgical intervention. Contraindications the transseptal approach is contraindicated in patients with left atrial thrombus or myxoma, or interatrial baffle patch. Reuse and/or repackaging may create a risk of patient or user infection, compromise the structural integrity and/or essential material and design characteristics of the device, which may lead to device failure, and/or lead to injury, illness or death of the patient. Precautions • Excessive bending, torquing, or kinking of the electrode catheter may cause damage to the catheter, including damage to the internal wires. Indications for use Bard Electrophysiologys Steerable Diagnostic Electrode Catheters are intended for temporary intracardiac sensing, recording, stimulation and temporary pacing during the evaluation of cardiac arrhythmias. Precautions • the safety and effectiveness of this device as an ablation catheter have not been established. Handle and dispose of in accordance with accepted medical practice and applicable local, state, and federal laws. The loop is controlled by the thumb-wheel mechanism on the handle, which causes the loop to expand or contract. The tip of the catheter, on which the loop resides, can also be curved in a single direction by pushing or pulling a slide tab on the handle. The transseptal approach is contraindicated in patients with left atrial thrombus or myxoma, or interatrial baffle patch. The retrograde transaortic approach is contraindicated due to the risk of entrapping the tip in the left ventricle. The induction of an unintended arrhythmia is a known complication of electrophysiologic procedures. Handle and dispose in accordance with accepted medical practice and applicable local, state and federal laws. The catheter handle has a slider mechanism which, when moved forward or back from the neutral position, results in curvature of the distal tip. Contraindications • the catheter should not be used in conditions where manipulation of the catheter would be unsafe (e. Warnings • this device should be used only by physicians thoroughly trained in the techniques of intracardiac electrophysiology studies and temporary pacing. The catheter handle has a rotary mechanism which, when rotated from the neutral position, results in curvature of the distal tip. Refer to the Instructions for Use for the complete List of Adverse Effects, Precautions, and Warning. Contraindications • Known active systemic or local infection • Known inability to obtain vascular access • Patients with atrial thrombus or myxoma, or interatrial baffle or patch • Use of a steerable sheath is contraindicated in patients with obstructed or inadequate vasculature. Warnings the steerable sheath must be thoroughly flushed with either saline or heparinized saline and free of air prior to use to avoid air embolism to the patient. If the patient has left bundle branch block, back up pacing should be readily available during insertion of the steerable sheath assembly. Before removing the steerable sheath, straighten the distal section as much as possible to avoid damage during removal. Precautions Transvenous device compatibility: Use the steerable sheath only with compatible transvenous devices. Use the appropriate size sheath for the size of the transvenous device being utilized. Consequences of using the steerable sheath with incompatible devices may include the inability to deliver the transvenous device or damage to the transvenous device during delivery. Do not aspirate steerable sheath with a guidewire in place through the hemostatic valve. The steerable sheath must be thoroughly flushed with either saline or heparinized saline and free of air prior to use to avoid air embolism to the patient. Stim Setup, including the stimulator connection settings, is stored with Amplifier Configuration nformation. Selecting a new Channel Setup could result in a change to the current stimulator pacing site(s). Defibrillation protection of hardware components can only be assured using cables and accessories supplied by Bard. Indications for Use the Stimulator system is an electrical stimulus generator for diagnostic cardiac stimulation during electrophysiological testing of the human heart. Contraindications Do not use the Stimulator system for life support in patients with life-threatening bradycardia; use instead temporary external pacemaker. Contact Micropace Pty Ltd for further information (Refer also to Warnings and Precautions section below). General Warnings Warning: Stimulator must be used only under supervision by a cardiologist. Cardiac Diagnostic Stimulators are used in medical procedures, during which intentional or unintentional life-threatening cardiac arrhythmias are likely to occur. To avoid death or injury to patient from arrhythmias, the Stimulator may be used on humans only under the direct supervision by a physician familiar with electrophysiology and the operation of this Stimulator, in an appropriate hospital facility. The supervising physician must verify all Stimulator settings immediately prior to commencement of pacing, with particular attention to any adaptively calculated S1 pacing interval settings, and in the case of StimLab™, in case settings were altered using the alternate controller.

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Outcome of seizures in the general population after 25 years: a prospective follow-up cheap simvastatin 40 mg fast delivery cholesterol medication with the least side effects, observational cohort study order 20mg simvastatin overnight delivery cholesterol test good bad. Predictors of multiple seizures in a cohort of children prospectively followed from the Prognosis in those with intractable epilepsy time of their frst unprovoked seizure buy simvastatin 40mg with visa cholesterol in shrimp how much. Seizure recurrence in adults after a newly diagnosed unprovoked epileptic seizure. Two-year remission and subsequent relapse in children with newly diagnosed epilepsy. A recent series of papers suggests, however, that such a view is overly Epilepsia 2001;42:1553–62. In a retrospective analysis of the effect of 265 medication changes in 155 patients with 11. Prognosis of epilepsy: a review and further analysis of the frst nine years of the British National General Practice Study of Epilepsy, a prospective population-based study. Remission of seizures in a population-based adult cohort with a newly diagnosed (12 months or more) following a drug introduction while a further 21% had a signifcant reduction unprovoked epileptic seizure. Natural history and prognosis of epilepsy: report of a multi-institutional study in Japan. The group In another study a group of 246 patients with refractory epilepsy was followed for three years. Long-term medical, educational, and social prognoses of childhood-onset retardation were statistically less likely to achieve a remission. Overall approximately 5% per year became epilepsy: a population-based study in a rural district of Japan. Natural history of treated childhood-onset epilepsy: prospective, long-term population-based a possibility of inducing meaningful seizure remission in this population47. Course and outcome of childhood epilepsy: a 15-year follow-up of the Dutch Study of Epilepsy in Childhood. The probability of seizure relapse following remission was retrospectively studied in a cohort of 20. Early seizure frequency and aetiology predict long-term medical outcome in childhood-onset 186 patients with intractable epilepsy who were followed for a median of 3. Patterns of relapse and remission in people achieved a remission of 12 months with a 4% probability of remission per year. First seizure presentation: do multiple seizures within 24 hours predict recurrence Factors predicting prognosis of epilepsy after presentation with In summary, approximately 45% a year of those with refractory epilepsy will achieve a remission seizures. Prognosis of epilepsy in newly referred patients: a multicenter prospective study of the effects of monotherapy on the long-term course of epilepsy. The overall prognosis for people with newly diagnosed epilepsy is good, with 7080% becoming seizure- 29. Seizure clustering during drug treatment affects seizure outcome and mortality of childhood-onset free, many of whom doing so in the early course of the condition. Does the cause of localisation-related epilepsy infuence the response to antiepileptic drug in appropriate candidates epilepsy surgery is four times more likely to render seizure freedom than treatment The characteristics of epilepsy in a largely untreated population in rural Ecuador. Comprehensive primary health care antiepileptic drug treatment programme in rural and semi-urban Kenya. Treatment of the frst tonic-clonic seizure does not affect long-term remission of epilepsy. Immediate versus deferred antiepileptic drug treatment for early epilepsy and single 1,2 3,4 seizures: a randomised controlled trial. Uncontrolled epilepsy following discontinuation of antiepileptic drugs in seizure-free patients: a review of current clinical experience. Consequences of antiepileptic drug withdrawal: a randomized, double-blind study (Akershus Study). Early surgical therapy for drug-resistant temporal lobe epilepsy: a randomised It has been consistently shown in population studies that the risk of premature death is two to three trial. Long-term seizure outcome of surgery versus no surgery for drug-resistant partial epilepsy: a review of controlled studies. The long-term outcome of adult epilepsy surgery, patterns of seizure remission, epilepsy and neurological defcits having persistently higher risks. Results of treatment changes in patients with apparently drug-resistant chronic epilepsy. Long-term population-based prospective incident cohort studies provide the most reliable means of 48. Seizure remission and relapse in adults with intractable epilepsy: a cohort study. Epilepsia 1 examining the risk of premature mortality and the way it changes over the course of the condition, 2008;49:1440–5. Treatment changes in a cohort of people with apparently drug-resistant epilepsy: although there are very few studies with follow-up of more than 20 years. The estimates of the risk of premature death have varied between studies, and case ascertainment can be an issue depending on the methodology used.

Pacing manoeuvres may result in the crista terminalis purchase simvastatin online pills cholesterol ratio significance, the atrial activation sequence will post overdrive acceleration generic 40 mg simvastatin with visa cholesterol test monitor. In the human ventricle buy simvastatin 20mg amex vldl cholesterol medication, not be very dierent from that during sinus rhythm or verapamil has been shown to suppress arrhythmia [29,30] inappropriate sinus tachycardia. Due to the rate with minor, but signicant changes in origin of lack of a reliable means of identifying these mechanisms activation detected by endocardial mapping permit in the electrophysiological laboratory, classication [37] diagnosis. Multiple atrial tachycardia foci have been solely on the basis of mechanisms is clinically very described, and can be a cause of recurrence after surgical dicult if not impossible, and currently is often clini- [38,39] or radiofrequency ablation. Thus, it will not be used in this proposal, Available information suggests that focal activity but will be addressed in each relevant situation. Over a prolonged period of observation (min- Mechanisms utes to hours), atrial tachycardia cycle length can exhibit important variations. A progressive rate increase at tachycardia onset (warm up)[40] and/or a progressive rate Focal atrial tachycardia is characterized by atrial acti- vation starting rhythmically at a small area (focus) decrease before tachycardia termination (cool down) Eur Heart J, Vol. After the impulse has propagated rapidly in all parts of both atria, an electrical silence follows until the next focal atrial discharge. Rate can bances, intra-atrial activation may extend over a large increase during exercise[41,42]. Typically, adrenergic proportion of the cycle length[43], and conduction spread stimulation can accelerate the rate of focal discharge. This point will be suggesting a reentrant mechanism, constant or progres- further discussed later. Collision of activation fronts and/or partial activation Mapping change during entrainment cannot be demonstrated with multiple endocardial recordings. There activation from the focus or origin may not be uniformly is a clearly dened isoelectric baseline between P waves radial, as conduction can be directed by anatomical or in all leads (Fig. There is generally focus location, and it can be used to approximately an electrically silent period in atrial cycle length that, in localize it before electrophysiological study[36]. Intra-cardiac mapping will show signicant recording can also be used to help localize the site of portions of the cycle length without recorded activity, origin of the tachycardia[44]. In this example of a 16-year-old girl, focal left atrial tachycardia with a cycle length of 480 ms originates in the lateral wall of the left atrium. In the presence of rapid rates and/or intra- pattern (continuous undulation without isoelectric atrial conduction disturbances, P waves can be very baseline). In the late post operative period after atrial septal defect closure, right atrial reentry with a cycle length of 420 ms occurs with the impulse rotating within a protected isthmus which is limited anteriorly by the tricuspid annulus and posteriorly by the atriotomy scar. Macroreentrant atrial tachycardia Mapping Mechanisms the reentry circuit includes large portions of the atria, where continuous, reentrant activation can be recorded the mechanism of macroreentrant atrial tachycardia is with detailed mapping. Activation should be recorded reentrant activation around a large central obstacle, continuously throughout the atrial tachycardia cycle generally several centimeters in diameter, at least in one length if atrial mapping is complete. The central obstacle may consist of ings will often show activation during isoelectric inter- normal or abnormal structures. For illustrative purposes, a particu- cardia mechanisms must be made in relation to atrial lar reference point may be designated as the origin of anatomy, including a detailed description of the activation (time 0), but it should be understood that this obstacles or boundaries of the circuit and the critical is always arbitrary[7,8]. Complex surgical procedures, isthmuses that may be targets for therapeutic action. Typical atrial utter, the most com- record activation throughout the cycle length. However conduction delays ridge)[7,9,10] are reected by recording double potentials within the circuit can prolong the atrial tachycardia (Fig. Double potentials express sequential activation cycle length, making it overlap with the classical focal on both sides of the line of block. The interpretation of ring after radiofrequency ablation and in atriotomy double potentials has to be made in the context of the macroreentrant atrial tachycardia. Double electrograms recorded from the centre of the circuit in a patient with scar macroreentrant tachycardia in the lateral right atrium. The superimposed schema represents a right anterior oblique view of the right atrium, and the clear band represents the scar. The bottom recording in each trace shows double electro- grams along the scarred area from superior to inferior, as marked in the schema. Note the decreasing separation of the electrogram components that become a continuous fraction- ated electrogram close to the inferior vena cava (L5), suggestive of local slow conduction. Macroreentry is conrmed if exact return pauses nents) electrogram identies a local dead-end pathway, (0–20 ms dierence from the baseline cycle length), are not essential for tachycardia mechanism (Fig. Mul- recorded from at least two atrial pacing sites, separated tiple component (fractionated) electrograms may be by at least 2 cm[17,48]. The entrainment cycle length recorded at sites of local conduction disturbances and/or should be of sucient length to prolong conduction, slow conduction[47]. Voltage mapping may be useful in which would result in a prolonged return cycle length, post surgical atrial tachycardia and in patients with even when pacing from within the circuit (Fig. Areas of low or absent local other hand, a very long entrainment cycle length makes electrogram amplitude in the bipolar mode represent it harder to recognize fusion/endocardial activation scar or patch material. The best characterized macroreentrant atrial tachy- cardias are typical (or isthmus dependant) atrial utters and atriotomy (or incisional) atrial tachycardia. Left Transient entrainment atrial macroreentrant atrial tachycardia are less well known due to the need for transeptal catheterization for Transient entrainment is possible in the vast majority of left atrial mapping. Some circuits are very unstable and pacing cycle length should be as close as possible to baseline cycle length in these cases. Mapping during typical atrial utter in a patient with severe local intra-atrial conduction disturbances. The distance between the two components of the rst double potential electrogram is 170 ms.

Diseases

  • Myoclonus ataxia
  • Odontophobia
  • Tsukuhara syndrome
  • CATCH 22 syndrome
  • Split hand split foot mandibular hypoplasia
  • Polymorphic catecholergic ventricular tachycardia
  • Cole carpenter syndrome

Approximately 35% of children with precedes the development of atopy46 and the modula- moderate and severe forms of the disease have food tion of the microenvironment can promote clinical allergies order 20mg simvastatin overnight delivery cholesterol vs triglycerides. In addition effective 10 mg simvastatin cholesterol levels in salmon, it also increases the produc- that 41% of the population had food allergy 10mg simvastatin for sale cholesterol ratio in india, identifying tion of IgA in the gut. Prevalencia de eczema atopico e sintomas relacionados entre increase protein and energy requirements. Atopic dermatitis disorders in children, including low weight and malnu- and nutrition. Eczema preva- lence in the United States: data from the 2003 National Survey of directly related to the number of food items to which Childrens Health. Folster-Holst R, Muller F, Schnopp N, Abeck D, Kreiselmaier the type of newborn feeding greatly influences their I, Lenz T et al. Prospective, randomized controlled trial on 55 Lactobacillus rhamnosus in infants with moderate to severe exposure to antigens. Guia Pratico para o Manejo da Dermatite Atopica – opiniao conjunta de especialistas em alergologia da diversity of antigens that have been ingested and Associacao Brasileira de Alergia e Imunopatologia e da Socie- processed by the mothers gastrointestinal tract, but with dade Brasileira de Pediatria. Rev Bras Alerg Imunopatol 2006; reduced allergenic potential, which contributes to the 29 (6): 268-82. Consensus Report of the four months or more, decreases the risk of developing European Task Force on Atopic Dermatitis. Epidemiology, clinical features, and immunology inverse relationship between early and transitory forms of the intrinsic (non-IgE-mediated) type of atopic dermatitis (constitutional dermatitis). Guidelines for the diagnosis and management of food as a protective factor for the development of the disease. Effect of probiotics on gastrointestinal symp- the food that should be offered to these children. Viljanen M, Savilahti E, Haahtela T, Juntunen-Backman K, microbiota of atopic children is different from that found Korpela R Poussa T et al. However, there are controversies eczema/dermatitis syndrome in infants: a double-blind about the widespread use of this alternative therapy in chil- placebo-controlled trial. It seems that children who have greater Probiotic supplement reduces atopic dermatitis in preschool benefit are those with a history of food allergies. Aberrant composition of gut microbiota of allergic infants: a target of fits of the use of probiotics as an adjunct in the treatment bifidobacterial therapy at weaning Probiotic bacteria in gastrointestinal microenvironment, especially in cases the management of atopic disease: underscoring the importance associated with food allergy. Clinical effects of probiotics are associated with increased altered skin barrier and immune dysregulation. Immunol Rev interferon-gamma responses in very young children with atopic 2011; 242 (1): 233-46. Probiotic effects on faecal inflamma- tratamento de doencas em lactentes e criancas. J Pediatr (Rio J) tory markers and on faecal IgA in food allergic atopic 2011; 87 (4): 292-300. Current level of consensus on probiotic science mechanism of probiotic effect in atopic eczema-dermatitis - report of an expert meeting -London, 23 November 2009. Characterizing the composition of atopic dermatitis in infancy: a randomized placebo-controlled intestinal microflora as a prospective treatment target in trial. The socioeconomic impact of the newborn and young children intestinal impact of atopic dermatitis in the United States: a systematic microflora. Verboom P, Hakkaart-Van L, Sturkenboom M, De Zeeuw R, prevention of pediatric antibiotic-associated diarrhea. The cost of atopic dermatitis in the Netherlands: Database of Systematic Reviews 2007, Issue 2, Art. Climate and the prevalence of according to sensitized food allergens in children with atopic symptoms of asthma, allergic rhinitis, and atopic eczema in dermatitis. Seasonality in symptom severity influenced by cuion del estado nutricional em ninos com dermatites atopica. Illi S, von Mutius E, Lau S, Nickel R, Gruber C, Niggemann B of atopic dermatitis during the first 3 years of life -results from the et al. Hypersensitivity should be suspected in the event of severe pruritus, swelling and erythema at the application site or at a distant site. The background risk of major birth defects and miscarriage for the indicated population is unknown. Data Animal Data Rat and rabbit embryo-fetal development was assessed after oral administration of crisaborole. Maternal toxicity was produced at the high dose of 600 mg/kg/day in pregnant rats and was associated with findings of decreased fetal body weight and delayed skeletal ossification. In a prenatal/postnatal development study, pregnant rats were treated with crisaborole at doses of 150, 300, and 600 mg/kg/day by oral gavage during gestation and lactation (from gestation day 7 through day 20 of lactation). Maternal toxicity was produced at the high dose of 600 mg/kg/day in pregnant rats and was associated with findings of stillbirths, pup mortality, and reduced pup weights. Crisaborole is described chemically as 5-(4-cyanophenoxy)-1,3-dihydro-1-hydroxy-[2,1]- benzoxaborole. The specific mechanism(s) by which crisaborole exerts its therapeutic action for the treatment of atopic dermatitis is not well defined. Distribution Based on an in vitro study, crisaborole is 97% bound to human plasma proteins. Elimination Metabolism Crisaborole is substantially metabolized into inactive metabolites.

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Mesial temporal temporal lobes discount simvastatin 40 mg on line cholesterol medication and orange juice, giving rise to the potential for false localiza- and lateral frontal seizure foci are the regions most amenable tion (25 cheap simvastatin 10 mg on line quest cholesterol test,27 buy simvastatin 40 mg line cholesterol levels in kfc,57,58). In general, the first 30–40 seconds of a seizure is unknown, but a factor may be the earlier interaction between provide the most useful localizing information. The seizure pattern in temporal lobe epilepsy where localized slowing can some- recorded in an individual patient with a single epileptogenic times be seen in the ipsilateral temporal region (80). Mesial temporal seizures typically are manifest as an should raise the possibility of a relatively large epileptogenic evolving rhythmic theta discharge arising over the ipsilateral zone or multiple seizure foci. A typical right mesial same brain region in different patients may show interindivid- temporal seizure is shown in Figure 74. C: the right temporal discharge fre- quency decreases toward the end of the seizure to the delta frequency range. D: Subtle lateralized postic- tal delta slowing and attenuation of the background is present over the right hemispheric derivations following seizure termination. At seizure termination, the discharge frequency fuse and is more apparent in seizures arising out of sleep (82). This is typically seen in diffuse, evolving into a more lateralized discharge over the seizures which spread from one hippocampus to the other ipsilateral temporal region after the first several seconds of the prior to propagation to the ipsilateral temporal neocortex. Mesial temporal depth electrode recordings may of a vertical dipole in the mesial temporal region with the be necessary to resolve seizure lateralization in such cases. In one study, the mean discharge fre- with mesial frontal seizures including generalized spike and quency at seizure onset in neocortical temporal seizures was wave, a diffuse electrodecremental pattern, and rhythmic ver- 1 Hz less than mesial temporal seizures (65). In the absence of a lar 5- to 9-Hz inferotemporal rhythm, and occasionally by a structural or functional imaging abnormality in such cases, vertex/parasagittal positive rhythm of the same frequency. In another series, mesial tempo- seizures may manifest as a focal low-amplitude high-frequency ral seizures were more likely to show fast rhythmic sharp discharge, an example of which is depicted in Figure 74. This can cause erroneous localiza- eate mesial and neocortical temporal seizures (44,62). Orbital However, intracranial monitoring is usually necessary when frontal seizures can also spread to other regions of the frontal definitive electrophysiologic clarification is required (46). A localizing ictal discharge may not be present in propagation to the temporal region (88). In one large surgical series, a local- ture that can reliably distinguish a propagated temporal dis- izing discharge at onset was seen over the temporo-occipital charge from a temporal origin rhythm (89). The parietal lobe is the least common area ing propagated versus temporal onset rhythms, but have not of seizure onset in partial epilepsy. Recognition of the various expressions of anxiety, psychosis, and aggression in epilepsy. Diagnosis and management of depression and psychosis in children and adolescents with epilepsy. Epileptic Seizures: Pathophysiology and Clinical surgery for temporal-lobe epilepsy [see comment]. Intracranial electroencephalog- electroencephalography and seizure semiology improves patient lateral- raphy seizure onset patterns and surgical outcomes in nonlesional ization in temporal lobe epilepsy. Recommendations regarding the require- ogy in distinguishing frontal lobe seizures and temporal lobe seizures. Improvement in the perfor- mesial temporal origin: electroclinical and metabolic patterns. State-dependent spike detection: concepts and functional connections of the living human brain. Ictal speech, postictal language dysfunction, and Electroencephalogr Clin Neurophysiol. Clinical and electrographic mani- partial seizures of temporal lobe onset: a new lateralizing sign [see com- festations of lesional neocortical temporal lobe epilepsy. Ictus emeticus: an electroclini- and electroencephalographic study of 46 pathologically proven cases. Occipital lobe epilepsy: rior temporal lobectomy for intractable epilepsy: a multivariate study. Noninvasive electroencephalography and mesial tem- effectiveness for intractable nonlesional focal epilepsy. Electroencephalographic studies of thalamic hamartomas: evaluation of patients undergoing chronic intracra- simple partial seizures with subdural electrode recordings. The value of closely spaced synchrony on recording scalp electroencephalography ictal patterns. J Neurol lobe origin: clinical characteristics, localizing signs, and results of surgery. Surgical management of malacias for intractable epilepsy: outcome and prognostic factors [see parietal lobe epilepsy. Although and to investigate the pathophysiology of partial and general- there are some individual differences in tracer distribution (1), ized seizure disorders. A tal regional decreases in glucose consumption that are invari- physiologic probe designed to assess a targeted function is ably ipsilateral to the seizure focus—typically, but not always, labeled with a radioactive tag. The few reports of false lateralization life of [15O]water renders it suitable for capturing the brief have occurred after surgery (3) was performed, when interpre- activity of cognitive processes. This may reflect the distant projection of func- result in misleading information and erroneous conclusions tional loss in mesial structures. Voxel-based statistical methods performed in a stan- contralateral hypometabolism appear to be reversible with dard anatomic atlas that allows comparison of individual successful temporal lobectomy (24).

References:

  • https://www.esvs.org/wp-content/uploads/2015/12/CLTI-Guidelines-ESVS-SVS-WFVS.pdf
  • https://read.dukeupress.edu/books/book/1560/chapter/173971/Misguided-Dangerous-and-WrongAn-Analysis-of
  • https://www.nrc.gov/docs/ML0224/ML022410238.pdf
  • http://cdn.intechopen.com/pdfs/34066/InTech-Modification_of_thermoplastics_with_reactive_silanes_and_siloxanes.pdf
  • https://www.pearson.com/content/dam/one-dot-com/one-dot-com/global/Files/sustainability/2018-reports/Pearson_2018_Sustainability_Report.pdf
 
 
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