1e
19
1
49
2
2
18
1b
1d
18
38
7b
1d
2 29
1d
25
Orith Waisbourd-Zinman, MD
88
7b
Adjunct Assistant Professor of Pediatrics (Gastroenterology, Hepatology and Nutrition)
7
61
Department: Pediatrics
4
1
b
1d
46
Contact information
5b
4
3
3
3
2
4
b
1f
5b
Schneider Children's Medical Center of Israel
3f 14 Kaplan Street, PO Box 559
Petach Tikvah 49202,
26
3f 14 Kaplan Street, PO Box 559
Petach Tikvah 49202,
35
f
13
Education:
21 9 BMSc c
5b Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, 2001.
21 7 MD c
5b Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, 2006.
c
3
3
3
3
8d
Permanent link21 9 BMSc c
5b Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, 2001.
21 7 MD c
5b Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel, 2006.
c
2 29
21
1e
1d
24
2b
29
27
23
f3 Wehrman A, Waisbourd-Zinman O, Shah A, Hilmara D, Lin H, Rand EB: Steroid Free Treatment of Autoimmune Hepatitis in Selected Children. J Pediatr 207: 244-247, April 2019.
e1 Wehrman A, Waisbourd-Zinman O, Wells RG: Recent advances in understanding biliary atresia. F1000Res Feb 2019 Notes: DOI: 10.12688/f1000research.16732.1
119 Assa A, Waisbourd-Zinman O, Daher S, Shamir R: Birth Month as a Risk Factor for the Diagnosis of Celiac Disease Later in Life: A Population-based Study. J Pediatr Gastroenterol Nutr 67(3): 367-370, Sep 2018.
18a Chen Y, Gilbert MA, Grochowski CM, McEldrew D, Llewellyn J, Waisbourd-Zinman O, Hakonarson H, Bailey-Wilson JE, Russo P, Wells RG, Loomes KM, Spinner NB, Devoto M: A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. PLoS Genet 14(8): e1007532, Aug 2018.
e2 Waisbourd-Zinman O, Shah A, Lin HC, Rand EB: Splenic Rupture in Children with Portal Hypertension. J Pediatr Gastroenterol Nutr 66(3): 447-450, Mar 2018.
115 Waisbourd-Zinman O, Surrey LF, Schwartz AE, Russo PA, Wen J: A novel BSEP mutation causes a mild form of progressive familial cholestasis type 2. Annals of Hepatology 2017 Notes: Accepted for publication.
111 Waisbourd-Zinman O, Surrey LF, Schwartz AE, Russo PA, Wen J: A Rare BSEP Mutation Associated with a Mild Form of Progressive Familial Intrahepatic Cholestasis Type 2. Ann Hepatol 16(3): 465-468, 2017.
11d Waisbourd-Zinman O: Reversibility of extra hepatic bile duct damage in biliary atresia, Poster presentation. Federation of American Societies for Experimental Biology Annual Meeting, West Palm Beach, FL Nov 2016.
119 Waisbourd-Zinman O: Primary sclerosing cholangitis and autoimmune hepatitis in sickle cell disease. Pediatric Gastroenterology, Hepatology and Nutrition, World Congress meeting, Montreal, Canada October 2016.
2c
7
1d
1f
Selected Publications
184 Zifman E, Waisbourd-Zinman O, Marderfeld L, Zevit N, guz-Mark A, Silbermintz A, Assa A, Mozer-Glassberg Y, Biran N, Reznik D, Poraz I, Shamir R: The effect of gluten-free diet on cardiovascular risk factors in newly diagnosed pediatric celiac disease patients. J Pediatr Gastroenterol Nutr 68(5): 684-688, May 2019.f3 Wehrman A, Waisbourd-Zinman O, Shah A, Hilmara D, Lin H, Rand EB: Steroid Free Treatment of Autoimmune Hepatitis in Selected Children. J Pediatr 207: 244-247, April 2019.
e1 Wehrman A, Waisbourd-Zinman O, Wells RG: Recent advances in understanding biliary atresia. F1000Res Feb 2019 Notes: DOI: 10.12688/f1000research.16732.1
119 Assa A, Waisbourd-Zinman O, Daher S, Shamir R: Birth Month as a Risk Factor for the Diagnosis of Celiac Disease Later in Life: A Population-based Study. J Pediatr Gastroenterol Nutr 67(3): 367-370, Sep 2018.
18a Chen Y, Gilbert MA, Grochowski CM, McEldrew D, Llewellyn J, Waisbourd-Zinman O, Hakonarson H, Bailey-Wilson JE, Russo P, Wells RG, Loomes KM, Spinner NB, Devoto M: A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. PLoS Genet 14(8): e1007532, Aug 2018.
e2 Waisbourd-Zinman O, Shah A, Lin HC, Rand EB: Splenic Rupture in Children with Portal Hypertension. J Pediatr Gastroenterol Nutr 66(3): 447-450, Mar 2018.
115 Waisbourd-Zinman O, Surrey LF, Schwartz AE, Russo PA, Wen J: A novel BSEP mutation causes a mild form of progressive familial cholestasis type 2. Annals of Hepatology 2017 Notes: Accepted for publication.
111 Waisbourd-Zinman O, Surrey LF, Schwartz AE, Russo PA, Wen J: A Rare BSEP Mutation Associated with a Mild Form of Progressive Familial Intrahepatic Cholestasis Type 2. Ann Hepatol 16(3): 465-468, 2017.
11d Waisbourd-Zinman O: Reversibility of extra hepatic bile duct damage in biliary atresia, Poster presentation. Federation of American Societies for Experimental Biology Annual Meeting, West Palm Beach, FL Nov 2016.
119 Waisbourd-Zinman O: Primary sclerosing cholangitis and autoimmune hepatitis in sickle cell disease. Pediatric Gastroenterology, Hepatology and Nutrition, World Congress meeting, Montreal, Canada October 2016.
2c