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Items: 1 to 20 of 27

1.

A Pilot Study to Reduce Central Line-Associated Bloodstream Infections in Children From Extremely Low-Income Settings With Intestinal Failure-Meeting the Challenge.

Fuchs I, Rosenbaum D, Klein I, Einhorn M, Pinsk V, Shelef Y, Sherf A, Press Y, Yerushalmi B.

J Pediatric Infect Dis Soc. 2019 Mar 13. pii: piz006. doi: 10.1093/jpids/piz006. [Epub ahead of print]

PMID:
30864666
2.

EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome.

Pathak SJ, Mueller JL, Okamoto K, Das B, Hertecant J, Greenhalgh L, Cole T, Pinsk V, Yerushalmi B, Gurkan OE, Yourshaw M, Hernandez E, Oesterreicher S, Naik S, Sanderson IR, Axelsson I, Agardh D, Boland CR, Martin MG, Putnam CD, Sivagnanam M.

Hum Mutat. 2019 Feb;40(2):142-161. doi: 10.1002/humu.23688. Epub 2018 Nov 29.

PMID:
30461124
3.

Seasonality of birth affects paediatric coeliac disease.

Daniel S, Kalansky A, Tsur A, Pinsk V, Ling G, Rannan R, Yerushalmi B.

Acta Paediatr. 2019 Mar;108(3):529-534. doi: 10.1111/apa.14441. Epub 2018 Jun 29.

PMID:
29885263
4.

Mycophenolate Mofetil Alone and in Combination with Tacrolimus Inhibits the Proliferation of HT-29 Human Colonic Adenocarcinoma Cell Line and Might Interfere with Colonic Tumorigenesis.

Ling G, Lamprecht S, Shubinsky G, Osyntsov L, Yerushalmi B, Pinsk I, Pinsk V, Ling E.

Anticancer Res. 2018 Jun;38(6):3333-3339. doi: 10.21873/anticanres.12599.

PMID:
29848681
5.

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.

Barzaghi F, Amaya Hernandez LC, Neven B, Ricci S, Kucuk ZY, Bleesing JJ, Nademi Z, Slatter MA, Ulloa ER, Shcherbina A, Roppelt A, Worth A, Silva J, Aiuti A, Murguia-Favela L, Speckmann C, Carneiro-Sampaio M, Fernandes JF, Baris S, Ozen A, Karakoc-Aydiner E, Kiykim A, Schulz A, Steinmann S, Notarangelo LD, Gambineri E, Lionetti P, Shearer WT, Forbes LR, Martinez C, Moshous D, Blanche S, Fisher A, Ruemmele FM, Tissandier C, Ouachee-Chardin M, Rieux-Laucat F, Cavazzana M, Qasim W, Lucarelli B, Albert MH, Kobayashi I, Alonso L, Diaz De Heredia C, Kanegane H, Lawitschka A, Seo JJ, Gonzalez-Vicent M, Diaz MA, Goyal RK, Sauer MG, Yesilipek A, Kim M, Yilmaz-Demirdag Y, Bhatia M, Khlevner J, Richmond Padilla EJ, Martino S, Montin D, Neth O, Molinos-Quintana A, Valverde-Fernandez J, Broides A, Pinsk V, Ballauf A, Haerynck F, Bordon V, Dhooge C, Garcia-Lloret ML, Bredius RG, KaƂwak K, Haddad E, Seidel MG, Duckers G, Pai SY, Dvorak CC, Ehl S, Locatelli F, Goldman F, Gennery AR, Cowan MJ, Roncarolo MG, Bacchetta R; Primary Immune Deficiency Treatment Consortium (PIDTC) and the Inborn Errors Working Party (IEWP) of the European Society for Blood and Marrow Transplantation (EBMT).

J Allergy Clin Immunol. 2018 Mar;141(3):1036-1049.e5. doi: 10.1016/j.jaci.2017.10.041. Epub 2017 Dec 11.

6.
7.

Management of Ingested Hijab-Pin.

Hubara E, Ling G, Pinsk V, Lior Y, Daniel S, Zuckerman S, Yerushalmi B.

J Gastrointest Surg. 2017 Jun;21(6):1062-1066. doi: 10.1007/s11605-017-3424-z. Epub 2017 Apr 19.

PMID:
28424984
8.

Incidence of typically Severe Primary Immunodeficiency Diseases in Consanguineous and Non-consanguineous Populations.

Broides A, Nahum A, Mandola AB, Rozner L, Pinsk V, Ling G, Yerushalmi B, Levy J, Givon-Lavi N.

J Clin Immunol. 2017 Apr;37(3):295-300. doi: 10.1007/s10875-017-0378-6. Epub 2017 Mar 16.

PMID:
28299599
9.

The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.

Broides A, Mandola AB, Levy J, Yerushalmi B, Pinsk V, Eldan M, Shubinsky G, Hadad N, Levy R, Nahum A, Ben-Harosh M, Lev A, Simon A, Somech R.

Immunol Res. 2017 Jun;65(3):651-657. doi: 10.1007/s12026-016-8883-x.

PMID:
28070732
10.

A case of cryopyrin-associated periodic fever syndrome due to Q703K mutation in the NLRP3 gene.

Ling E, Ling G, Pinsk V.

Int J Rheum Dis. 2017 Dec;20(12):2233-2235. doi: 10.1111/1756-185X.12991. Epub 2016 Dec 12. No abstract available.

PMID:
27943647
11.

Subclinical intestinal inflammation in chronic granulomatous disease patients.

Broides A, Sagi O, Pinsk V, Levy J, Yerushalmi B.

Immunol Res. 2016 Feb;64(1):155-9. doi: 10.1007/s12026-015-8733-2.

PMID:
26603166
12.

Acute Liver Failure in a Pediatric Patient with Congenital Dysery-Thropoietic Anemia Type I Treated with Deferasirox.

Ling G, Pinsk V, Golan-Tripto I, Ling E.

Hematol Rep. 2015 Sep 23;7(3):5987. doi: 10.4081/hr.2015.5987. eCollection 2015 Sep 23.

13.

Variation of muscular structure in congenital insensitivity to pain and anhidrosis.

Shorer Z, Shaco-Levy R, Pinsk V, Kachko L, Levy J.

Pediatr Neurol. 2013 Apr;48(4):311-3. doi: 10.1016/j.pediatrneurol.2012.12.015. Review.

PMID:
23498566
14.

Abnormal neutrophil chemotactic activity in children with congenital insensitivity to pain with anhidrosis (CIPA): the role of nerve growth factor.

Beigelman A, Levy J, Hadad N, Pinsk V, Haim A, Fruchtman Y, Levy R.

Clin Immunol. 2009 Mar;130(3):365-72. doi: 10.1016/j.clim.2008.09.005. Epub 2008 Oct 26.

PMID:
18955016
15.

Efficacy and safety of intravenous iron sucrose therapy in a group of children with iron deficiency anemia.

Pinsk V, Levy J, Moser A, Yerushalmi B, Kapelushnik J.

Isr Med Assoc J. 2008 May;10(5):335-8.

16.

Surgical intervention in children with Crohn's disease.

Leonor R, Jacobson K, Pinsk V, Webber E, Lemberg DA.

Int J Colorectal Dis. 2007 Sep;22(9):1037-41. Epub 2007 Feb 14. Review.

PMID:
17530264
17.

Inflammatory bowel disease in the South Asian pediatric population of British Columbia.

Pinsk V, Lemberg DA, Grewal K, Barker CC, Schreiber RA, Jacobson K.

Am J Gastroenterol. 2007 May;102(5):1077-83. Epub 2007 Mar 22.

PMID:
17378907
18.

Decreased first phase insulin response in children with congenital insensitivity to pain with anhidrosis.

Schreiber R, Levy J, Loewenthal N, Pinsk V, Hershkovitz E.

J Pediatr Endocrinol Metab. 2005 Sep;18(9):873-7.

PMID:
16279365
19.

[Clinical and genetic aspects of congenital insensitivity to pain with anhidrosis].

Schwarzkopf R, Pinsk V, Weisel Y, Atar D, Gorzak Y.

Harefuah. 2005 Jun;144(6):433-7, 453, 452. Review. Hebrew.

PMID:
15999564
20.

Nerve growth factor-tyrosine kinase A pathway is involved in thermoregulation and adaptation to stress: studies on patients with hereditary sensory and autonomic neuropathy type IV.

Loewenthal N, Levy J, Schreiber R, Pinsk V, Perry Z, Shorer Z, Hershkovitz E.

Pediatr Res. 2005 Apr;57(4):587-90. Epub 2005 Feb 4.

PMID:
15695606

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