 David Chin, MD
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| Title | Resident Physician |
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| Institution | University of California San Francisco |
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| Department | Anesthesia |
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| Address | 513 Parnassus Avenue
San Francisco CA 94117
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| vCard | Download vCard |
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 Biography | Rutgers New Jersey Medical School, Newark, NJ | MD | 05/2018 | Medicine | | Georgetown University, Washington, DC | BS | 05/2012 | Biology |
Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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Amin MD, Chin D, Amin S, Patel A.Anesthetic Challenges in a Child with Pulmonary Agenesis: A Case Report and Review of Literature. Journal of Anesthesia and Clinical Research. 2018; 6(9).
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Diep J, Chin D, Gupta S, Syed F, Xiong M, Cheng J. Kratom, an Emerging Drug of Abuse: A Case Report of Overdose and Management of Withdrawal. A A Pract. 2018 Apr 15; 10(8):192-194. PMID: 29652682.
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Amin M, Diep J, Chin D, Kahn JA, Monteiro I, Jackson D, Shulman SM .The Use of Smartphone Video Feature for Diagnosis and Counseling of a Propofol-Induced Acute Dystonic Reaction in a Pediatric Patient. Journal of Clinical Anesthesia and Management. 2017; 2(2).
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Zhou Q, Wang H, Schwartz DM, Stoffels M, Park YH, Zhang Y, Yang D, Demirkaya E, Takeuchi M, Tsai WL, Lyons JJ, Yu X, Ouyang C, Chen C, Chin D, Zaal K, Chandrasekharappa SC, P Hanson E, Yu Z, Mullikin JC, Hasni SA, Wertz IE, Ombrello AK, Stone DL, Hoffmann P, Jones A, Barham BK, Leavis HL, van Royen-Kerkof A, Sibley C, Batu ED, Gül A, Siegel RM, Boehm M, Milner JD, Ozen S, Gadina M, Chae J, Laxer RM, Kastner DL, Aksentijevich I. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease. Nat Genet. 2016 Jan; 48(1):67-73. PMID: 26642243.
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Zhou Q, Yang D, Ombrello AK, Zavialov AV, Toro C, Zavialov AV, Stone DL, Chae JJ, Rosenzweig SD, Bishop K, Barron KS, Kuehn HS, Hoffmann P, Negro A, Tsai WL, Cowen EW, Pei W, Milner JD, Silvin C, Heller T, Chin D, Patronas NJ, Barber JS, Lee CC, Wood GM, Ling A, Kelly SJ, Kleiner DE, Mullikin JC, Ganson NJ, Kong HH, Hambleton S, Candotti F, Quezado MM, Calvo KR, Alao H, Barham BK, Jones A, Meschia JF, Worrall BB, Kasner SE, Rich SS, Goldbach-Mansky R, Abinun M, Chalom E, Gotte AC, Punaro M, Pascual V, Verbsky JW, Torgerson TR, Singer NG, Gershon TR, Ozen S, Karadag O, Fleisher TA, Remmers EF, Burgess SM, Moir SL, Gadina M, Sood R, Hershfield MS, Boehm M, Kastner DL, Aksentijevich I. Early-onset stroke and vasculopathy associated with mutations in ADA2. N Engl J Med. 2014 Mar 06; 370(10):911-20. PMID: 24552284.
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Zhou Q, Laxer R, Pelletier M, Ramaswamy M, Wang H-Y, Chin D, Gül A, Sibley C, Barat-Houari M, Siegel R, Kastner DL, Aksentijevich I.Exome Sequencing in Monogenic Behçet-like Disease. Pediatric Rheumatology Online Journal. 2013; (11).
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Zhou Q, Ombrello AK, Chin D, Kastner DL, Aksentijevich I.Pediatric Rheumatology Online Journal. NLRP3 mosaicism as a cause of late-onset CAPS. 2013; (11).
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Zhou Q, Zavialov A, Chae J, Hershfield M, Sood R, Burgess S, Zavialov A, Chin D, Gadina M, Goldbach-Mansky R, Ombrello A, Stone D, Aksentijevich I, Kastner D.Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes. 2013.
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