Schreiber R - Search Results

1

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

Schreiber R, Levy J, Loewenthal N, Pinsk V, Hershkovitz E. Schreiber R, et al. J Pediatr Endocrinol Metab. 2005 Sep;18(9):873-7. doi: 10.1515/jpem.2005.18.9.873. J Pediatr Endocrinol Metab. 2005. PMID: 16279365

2

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. Loewenthal N, et al. Among authors: schreiber r. Pediatr Res. 2005 Apr;57(4):587-90. doi: 10.1203/01.PDR.0000155941.37155.41. Epub 2005 Feb 4. Pediatr Res. 2005. PMID: 15695606

3

Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical center.

David O, Agur R, Novoa R, Shaki D, Walker D, Carmon L, Eskin-Schwartz M, Birk OS, Ling G, Schreiber R, Loewenthal N, Haim A, Hershkovitz E. David O, et al. Among authors: schreiber r. Front Pediatr. 2022 Jul 22;10:916679. doi: 10.3389/fped.2022.916679. eCollection 2022. Front Pediatr. 2022. PMID: 35935360 Free PMC article.

4

Glomerular involvement in children with H syndrome.

David O, Geylis M, Kristal E, Ling G, Schreiber R. David O, et al. Among authors: schreiber r. Pediatr Nephrol. 2021 Mar;36(3):721-724. doi: 10.1007/s00467-020-04860-5. Epub 2021 Jan 2. Pediatr Nephrol. 2021. PMID: 33387019

5

Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.

Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, Koneth I, Schiffer M, Anikster Y, Hildebrandt F. Vivante A, et al. Among authors: schreiber r. Pediatr Nephrol. 2019 Sep;34(9):1607-1613. doi: 10.1007/s00467-019-04256-0. Epub 2019 Apr 17. Pediatr Nephrol. 2019. PMID: 31001663 Free PMC article.

6

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.

Perez Y, Shorer Z, Liani-Leibson K, Chabosseau P, Kadir R, Volodarsky M, Halperin D, Barber-Zucker S, Shalev H, Schreiber R, Gradstein L, Gurevich E, Zarivach R, Rutter GA, Landau D, Birk OS. Perez Y, et al. Among authors: schreiber r. Brain. 2017 Apr 1;140(4):928-939. doi: 10.1093/brain/awx013. Brain. 2017. PMID: 28334855 Free PMC article.

7

Brachial artery pseudoaneurysm in a premature infant.

Landau D, Schreiber R, Szendro G, Golcman L. Landau D, et al. Among authors: schreiber r. Arch Dis Child Fetal Neonatal Ed. 2003 Mar;88(2):F152-3. doi: 10.1136/fn.88.2.f152. Arch Dis Child Fetal Neonatal Ed. 2003. PMID: 12598507 Free PMC article.

8

Inherited renal tubular dysgenesis may not be universally fatal.

Schreiber R, Gubler MC, Gribouval O, Shalev H, Landau D. Schreiber R, et al. Pediatr Nephrol. 2010 Dec;25(12):2531-4. doi: 10.1007/s00467-010-1584-0. Epub 2010 Jul 6. Pediatr Nephrol. 2010. PMID: 20607303

9

Hodgkin's lymphoma, nephrotic syndrome, and echinococcosis cysts: an unusual association and literature review.

Geylis M, Rosen GB, Danino D, Schreiber R, Hassan D, Nalbandyan K, Nahum A. Geylis M, et al. Among authors: schreiber r. Pediatr Hematol Oncol. 2019 Feb;36(1):40-45. doi: 10.1080/08880018.2019.1571541. Epub 2019 Feb 20. Pediatr Hematol Oncol. 2019. PMID: 30784346 Review.

10

[RENAL TUBULAR DYSGENESIS SECONDARY TO MUTATIONS IN GENES ENCODING THE RENIN-ANGIOTENSIN SYSTEM].

Schreiber R, Dolgin V, Landau D, Gurevich E, Shalev H, Geylis M. Schreiber R, et al. Harefuah. 2021 Dec;160(12):822-826. Harefuah. 2021. PMID: 34957720 Hebrew.

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