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	1.	Iatrogenic Cushing Syndrome due to Intranasal Dexamethasone. [electronic resource] by Rottenstreich, Amihai Wexler, Isaiah D Abu-Libdeh, Abdulsalam Berkun, Yackov Producer: 20160503 In: Clinical pediatrics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Optimizing health care for individuals with Down syndrome in Israel. [electronic resource] by Wexler, Isaiah D Abu-Libdeh, Abdulsalam Kastiel, Yael Nimrodi, Alon Kerem, Eitan Tenenbaum, Ariel Producer: 20100225 In: The Israel Medical Association journal : IMAJ vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	3.	Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy. [electronic resource] by Abu Libdeh, Abdulsalam Levy-Khademi, Floris Abdulhadi-Atwan, Maha Bosin, Emily Korner, Mira White, Perrin C Zangen, David H Producer: 20100217 In: European journal of endocrinology vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence. [electronic resource] by Abdulhadi-Atwan, Maha Bushman, Jeremy Bushmann, Jeremy Tornovsky-Babaey, Sharona Perry, Avital Abu-Libdeh, Abdulsalam Glaser, Benjamin Shyng, Show-Ling Zangen, David H Producer: 20080801 In: Diabetes vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	RETRACTED: Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation. [electronic resource] by Molho-Pessach, Vered Ramot, Yuval Mogilevsky, Maxim Cohen-Daniel, Leonor Eisenstein, Eli M Abu-Libdeh, Abdulsalam Siam, Ihab Berger, Michael Karni, Rotem Zlotogorski, Abraham Producer: 20180412 In: Journal of dermatological science vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Propionic acidemia mimicking diabetic ketoacidosis. [electronic resource] by Dweikat, Imad M Naser, Enas N Abu Libdeh, Abdulsalam I Naser, Osama J Abu Gharbieh, Najwan N Maraqa, Nizar F Abu Libdeh, Bassam Y Producer: 20110815 In: Brain & development vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Familial autosomal recessive renal tubular acidosis: importance of early diagnosis. [electronic resource] by Vivante, Asaf Lotan, Danny Pode-Shakked, Naomi Landau, Daniel Svec, Peter Nampoothiri, Sheela Verma, Ishwar Abu-Libdeh, Abdulsalam Bockenhauer, Detlef Dekel, Benjamin Anikster, Yair Producer: 20140407 In: Nephron. Physiology vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress. [electronic resource] by Weinberg-Shukron, Ariella Abu-Libdeh, Abdulsalam Zhadeh, Fouad Carmel, Liran Kogot-Levin, Aviram Kamal, Lara Kanaan, Moien Zeligson, Sharon Renbaum, Paul Levy-Lahad, Ephrat Zangen, David Producer: 20160602 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription. [electronic resource] by Zangen, David Kaufman, Yotam Zeligson, Sharon Perlberg, Shira Fridman, Hila Kanaan, Moein Abdulhadi-Atwan, Maha Abu Libdeh, Abdulsalam Gussow, Ayal Kisslov, Irit Carmel, Liran Renbaum, Paul Levy-Lahad, Ephrat Producer: 20111212 In: American journal of human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome. [electronic resource] by Danielpur, Liron Sohn, Yang-Sung Karmi, Ola Fogel, Chen Zinger, Adar Abu-Libdeh, Abdulsalam Israeli, Tal Riahi, Yael Pappo, Orit Birk, Ruth Zangen, David H Mittler, Ron Cabantchik, Zvi-Ioav Cerasi, Erol Nechushtai, Rachel Leibowitz, Gil Producer: 20170630 In: The Journal of clinical endocrinology and metabolism vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Combined Gestational Age- and Birth Weight-Adjusted Cutoffs for Newborn Screening of Congenital Adrenal Hyperplasia. [electronic resource] by Pode-Shakked, Naomi Blau, Ayala Pode-Shakked, Ben Tiosano, Dov Weintrob, Naomi Eyal, Ori Zung, Amnon Levy-Khademi, Floris Tenenbaum-Rakover, Yardena Zangen, David Gillis, David Pinhas-Hamiel, Orit Loewenthal, Neta de Vries, Liat Landau, Zohar Rachmiel, Mariana Abu-Libdeh, Abdulsalam Eliakim, Alon Strich, David Koren, Ilana German, Alina Sack, Joseph Almashanu, Shlomo Producer: 20200520 In: The Journal of clinical endocrinology and metabolism vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)