David O - Search Results

1

Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy.

David O, Eskin-Schwartz M, Ling G, Dolgin V, Kristal E, Benkowitz E, Osyntsov L, Gradstein L, Birk OS, Loewenthal N, Yerushalmi B. David O, et al. Clin Genet. 2020 Sep;98(3):303-307. doi: 10.1111/cge.13805. Epub 2020 Aug 3. Clin Genet. 2020. PMID: 32617964

2

Diagnosis, Management, and Possible Prevention of Hungry Bone Syndrome in an Adolescent with Primary Hyperparathyroidism and Vitamin D Deficiency.

David O, Loewenthal N, Haim A, Makarov V, Hershkovitz E. David O, et al. Isr Med Assoc J. 2020 Feb;22(2):122-124. Isr Med Assoc J. 2020. PMID: 32043332 Free article. No abstract available.

3

Multiple Endocrine Deficiencies are Common in Hypoparathyroidism-Retardation-Dysmorphism Syndrome.

David O, Barash G, Agur R, Loewenthal N, Carmon L, Shaki D, Walker D, Novoa R, Haim A, Hershkovitz E. David O, et al. J Clin Endocrinol Metab. 2021 Jan 23;106(2):e907-e916. doi: 10.1210/clinem/dgaa807. J Clin Endocrinol Metab. 2021. PMID: 33150438 Clinical Trial.

4

Glomerular involvement in children with H syndrome.

David O, Geylis M, Kristal E, Ling G, Schreiber R. David O, et al. 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

The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel.

Kristal E, Pode-Shakked B, Hazan G, Banne E, Ling G, David O, Shany E, Raas-Rothschild A, Anikster Y, Kneller K, Hershkovitz E, Landau YE, Spiegel R, Zehavi Y, Staretz-Chacham O. Kristal E, et al. Among authors: david o. Orphanet J Rare Dis. 2021 Sep 8;16(1):379. doi: 10.1186/s13023-021-02007-9. Orphanet J Rare Dis. 2021. PMID: 34496908 Free PMC article.

6

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. Front Pediatr. 2022 Jul 22;10:916679. doi: 10.3389/fped.2022.916679. eCollection 2022. Front Pediatr. 2022. PMID: 35935360 Free PMC article.

7

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

David O, Kristal E, Ling G, Broides A, Hadad N, Shubinsky G, Nahum A. David O, et al. J Clin Immunol. 2023 Feb;43(2):350-357. doi: 10.1007/s10875-022-01380-9. Epub 2022 Oct 18. J Clin Immunol. 2023. PMID: 36258138 Free PMC article.

8

GHRH-GH-IGF1 axis in pediatric Down syndrome: A systematic review and mini meta-analysis.

Shaki D, Hershkovitz E, Tamam S, Bollotin A, David O, Yalovitsky G, Loewenthal N, Carmon L, Walker D, Haim A. Shaki D, et al. Among authors: david o. Front Pediatr. 2023 Feb 22;11:1132296. doi: 10.3389/fped.2023.1132296. eCollection 2023. Front Pediatr. 2023. PMID: 36911030 Free PMC article.

9

GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysis.

Shaki D, Hershkovitz E, Tamam S, Bollotin A, David O, Yalovitsky G, Loewenthal N, Carmon L, Walker D, Nowak R, Haim A. Shaki D, et al. Among authors: david o. Front Endocrinol (Lausanne). 2023 Apr 21;14:1135768. doi: 10.3389/fendo.2023.1135768. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37152958 Free PMC article.

10

Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signaling.

Shiloh R, Lubin R, David O, Geron I, Okon E, Hazan I, Zaliova M, Amarilyo G, Birger Y, Borovitz Y, Brik D, Broides A, Cohen-Kedar S, Harel L, Kristal E, Kozlova D, Ling G, Shapira Rootman M, Shefer Averbuch N, Spielman S, Trka J, Izraeli S, Yona S, Elitzur S. Shiloh R, et al. Among authors: david o. Blood. 2023 Nov 16;142(20):1740-1751. doi: 10.1182/blood.2023020714. Blood. 2023. PMID: 37738562

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