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Multiple Endocrine Deficiencies are Common in Hypoparathyroidism–Retardation–Dysmorphism Syndrome.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2021, v. 106, n. 2, p. e907, doi. 10.1210/clinem/dgaa807
By:
- David, Odeya;
- Barash, Galia;
- Agur, Rotem;
- Loewenthal, Neta;
- Carmon, Lior;
- Shaki, David;
- Walker, Dganit;
- Novoa, Rosa;
- Haim, Alon;
- Hershkovitz, Eli
Publication type:
Article
Diagnostic Yield of Critical Sample and Elective Fast-Test in Children After a Hypoglycemic Event: Experience From a Single Center in Israel.
Published in:
Indian Pediatrics, 2024, v. 61, n. 4, p. 348, doi. 10.1007/s13312-024-3157-5
By:
- Carmon, Lior;
- Hazan, Ran;
- Hershkovitz, Eli;
- David, Odeya;
- Shaki, David;
- Walker, Dganit;
- Loewenthal, Neta;
- Nasar, Majd;
- Hazan, Guy;
- Haim, Alon
Publication type:
Article
GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysis.
Published in:
Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1135768
By:
- Shaki, David;
- Hershkovitz, Eli;
- Tamam, Shai;
- Bollotin, Arkadi;
- David, Odeya;
- Yalovitsky, Guy;
- Loewenthal, Neta;
- Carmon, Lior;
- Walker, Dganit;
- Nowak, Raphael;
- Haim, Alon
Publication type:
Article
The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel.
Published in:
2021
By:
- Kristal, Eyal;
- Pode-Shakked, Ben;
- Hazan, Guy;
- Banne, Ehud;
- Ling, Galina;
- David, Odeya;
- Shany, Eilon;
- Raas-Rothschild, Annick;
- Anikster, Yair;
- Kneller, Katya;
- Hershkovitz, Eli;
- Landau, Yuval E.;
- Spiegel, Ronen;
- Zehavi, Yoav;
- Staretz-Chacham, Orna
Publication type:
journal article
Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy.
Published in:
Clinical Genetics, 2020, v. 98, n. 3, p. 303, doi. 10.1111/cge.13805
By:
- David, Odeya;
- Eskin‐Schwartz, Marina;
- Ling, Galina;
- Dolgin, Vadim;
- Kristal, Eyal;
- Benkowitz, Ela;
- Osyntsov, Lidia;
- Gradstein, Libe;
- Birk, Ohad S.;
- Loewenthal, Neta;
- Yerushalmi, Baruch
Publication type:
Article
Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.
Published in:
Journal of Clinical Immunology, 2023, v. 43, n. 2, p. 350, doi. 10.1007/s10875-022-01380-9
By:
- David, Odeya;
- Kristal, Eyal;
- Ling, Galina;
- Broides, Arnon;
- Hadad, Nurit;
- Shubinsky, George;
- Nahum, Amit
Publication type:
Article
Glomerular involvement in children with H syndrome.
Published in:
Pediatric Nephrology, 2021, v. 36, n. 3, p. 721, doi. 10.1007/s00467-020-04860-5
By:
- David, Odeya;
- Geylis, Michael;
- Kristal, Eyal;
- Ling, Galina;
- Schreiber, Ruth
Publication type:
Article
Alarming increase in ketoacidosis in children and adolescents with newly diagnosed type 1 diabetes during the first wave of the COVID‐19 pandemic in Israel.
Published in:
Pediatric Diabetes, 2022, v. 23, n. 1, p. 10, doi. 10.1111/pedi.13296
By:
- Goldman, Shira;
- Pinhas‐Hamiel, Orit;
- Weinberg, Adi;
- Auerbach, Adi;
- German, Alina;
- Haim, Alon;
- Zung, Amnon;
- Brener, Avivit;
- Strich, David;
- Azoulay, Erez;
- Levy‐Khademi, Floris;
- Ludar, Hanna;
- Koren, Ilana;
- Rachmiel, Marianna;
- Yackobovitch‐Gavan, Michal;
- Zuckerman‐Levin, Nehama;
- David, Odeya;
- Halloun, Rana;
- Cahn, Ranit;
- Ben‐Ari, Tal
Publication type:
Article
Diagnosis, Management, and Possible Prevention of Hungry Bone Syndrome in an Adolescent with Primary Hyperparathyroidism and Vitamin D Deficiency.
Published in:
Israel Medical Association Journal, 2020, v. 22, n. 2, p. 122
By:
- David, Odeya;
- Loewenthal, Neta;
- Haim, Alon;
- Makarov, Victoria;
- Hershkovitz, Eli
Publication type:
Article

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