1. Phosphoglucomutase‐1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiency. (19th August 2015) Authors: Loewenthal, Neta; Haim, Alon; Parvari, Ruti; Hershkovitz, Eli Journal: American journal of medical genetics Issue: Volume 167:Number 12(2015:Dec.) Page Start: 3139 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Antenatal diagnosis and treatment of hypothyroid fetal goiter in an euthyroid mother: a case report and review of literature. (12th December 2015) Authors: Mastrolia, Salvatore Andrea; Mandola, Amarilla; Mazor, Moshe; Hershkovitz, Reli; Mesner, Oded; Beer-Weisel, Ruthy; Besser, Limor; Shelef, Ilan; Loewenthal, Neta; Golan, Agneta; Gruzman, Igor; Erez, Offer Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 28:Number 18(2015) Page Start: 2214 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Visits at the primary clinic do not reduce ketoacidosis rates at presentation in type 1 diabetes mellitus. (14th September 2020) Authors: Yona, Assaf; Haim, Alon; Friger, Michael; Chechik, Tzila Gartzia; Loewenthal, Neta; Hershkovitz, Eli Journal: Acta pædiatrica Issue: Volume 110:Number 3(2021) Page Start: 995 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Long-term safety of α-1 antitrypsin therapy in children and adolescents with Type 1 diabetes. (21st September 2018) Authors: Brener, Avivit; Lebenthal, Yael; Interator, Hagar; Horesh, Orit; Leshem, Avital; Weintrob, Naomi; Loewenthal, Neta; Shalitin, Shlomit; Rachmiel, Marianna Journal: Immunotherapy Issue: Volume 10:Number 13(2018) Page Start: 1137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Birth during the moderate weather seasons is associated with early onset of type 1 diabetes in the Mediterranean area. Issue 7 (19th April 2020) Authors: Adar, Adi; Shalitin, Shlomit; Eyal, Ori; Loewenthal, Neta; Pinhas‐Hamiel, Orit; Zuckerman Levin, Nehama; Dally‐Gottfried, Orna; Landau, Zohar; Zung, Amnon; Levy‐Khademi, Floris; Zangen, David; Tenenbaum‐Rakover, Yardena; Rachmiel, Marianna Journal: Diabetes/metabolism research and reviews Issue: Volume 36:Issue 7(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The effect of vitamin D administration on vitamin D status and respiratory morbidity in late premature infants. Issue 11 (12th August 2020) Authors: Golan‐Tripto, Inbal; Bistritzer, Jacob; Loewenthal, Neta; Staretz‐Chacham, Orna; Dizitzer, Yotam; Goldbart, Aviv Journal: Pediatric pulmonology Issue: Volume 55:Issue 11(2020) Page Start: 3080 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. Issue 3 (3rd August 2020) Authors: David, Odeya; Eskin‐Schwartz, Marina; Ling, Galina; Dolgin, Vadim; Kristal, Eyal; Benkowitz, Ela; Osyntsov, Lidia; Gradstein, Libe; Birk, Ohad S.; Loewenthal, Neta; Yerushalmi, Baruch Journal: Clinical genetics Issue: Volume 98:Issue 3(2020) Page Start: 303 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prevalence of early and late prematurity is similar among pediatric type 1 diabetes patients and the general population. Issue 5 (24th March 2018) Authors: Adar, Adi; Shalitin, Shlomit; Eyal, Ori; Loewenthal, Neta; Pinhas‐Hamiel, Orit; Levy, Milana; Dally‐Gottfried, Orna; Landau, Zohar; Zung, Amnon; Levy‐Khademi, Floris; Zangen, David; Tenenbaum‐Rakover, Yardena; Rachmiel, Marianna Journal: Diabetes/metabolism research and reviews Issue: Volume 34:Issue 5(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Essential role of carbonic anhydrase XII in secretory gland fluid and HCO3− secretion revealed by disease causing human mutation. (7th December 2015) Authors: Hong, Jeong Hee; Muhammad, Emad; Zheng, Changyu; Hershkovitz, Eli; Alkrinawi, Soliman; Loewenthal, Neta; Parvari, Ruti; Muallem, Shmuel Journal: Journal of physiology Issue: Volume 593:Number 24(2015:Dec.) Page Start: 5299 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux–Lamy syndrome (MPS VI). Issue 12 (26th August 2021) Authors: Marek‐Yagel, Dina; Eliyahu, Aviva; Veber, Alvit; Shalva, Nechama; Philosoph, Amit Mary; Barel, Ortal; Javasky, Elisheva; Pode‐Shakked, Ben; Loewenthal, Neta; Anikster, Yair; Staretz‐Chacham, Orna Journal: American journal of medical genetics Issue: Volume 185:Issue 12(2021) Page Start: 3804 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗