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Search Results - Shalev, Hana
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Reduction in the prevalence of anemia in Bedouin infants, aged 9-18 months, in Southern Israel
by
Shalev, Hana
,
Urkin, Jacob
Published in
International public health journal
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Pediatricians' perspective on the challenges of care for Bedouin children in Southern Israel
by
Urkin, Jacob
,
Elsana, Foad
,
Elbedour, Khalil
,
Shalev, Hana
Published in
International public health journal
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Human Autosomal Recessive Osteopetrosis Maps to 11q13, a Position Predicted by Comparative Mapping of the Murine Osteosclerosis (oc) Mutation
by
Heaney, Conor
,
Shalev, Hana
,
Elbedour, Khalil
,
Carmi, Rivka
,
Staack, Jeffrey B.
,
Sheffield, Val C.
,
Beier, David R.
Published in
Human molecular genetics
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A Bedouin Kindred with Infantile Nephronophthisis Demonstrates Linkage to Chromosome 9 by Homozygosity Mapping
by
Haider, Neena B.
,
Carmi, Rivka
,
Shalev, Hana
,
Sheffield, Val C.
,
Landau, Daniel
Published in
American journal of human genetics
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Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p
by
Brennan, Theresa M.H.
,
Landau, Daniel
,
Shalev, Hana
,
Lamb, Fred
,
Schutte, Brian C.
,
Walder, Roxanne Y.
,
Mark, Allyn L.
,
Carmi, Rivka
,
Sheffield, Val C.
Published in
American journal of human genetics
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Geriatric Psychiatrists’ Perspectives on Palliative Care: Results From A National Survey
by
Elhassan, Hana
,
Robbins-Welty, Gregg A.
,
Moxley, Jerad
,
Reid, M. Carrington
,
Shalev, Daniel
Published in
Journal of geriatric psychiatry and neurology
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Digital resampling diversity sparsity constrained-wavefield reconstruction using single-magnitude image
by
Rivenson, Yair
,
Aviv Shalev, Maya
,
Weiss, Aryeh
,
Panet, Hana
,
Zalevsky, Zeev
Published in
Optics letters
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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1
by
Brownstein, Zippora
,
Gulsuner, Suleyman
,
Walsh, Tom
,
Martins, Fábio T.A.
,
Taiber, Shahar
,
Isakov, Ofer
,
Lee, Ming K.
,
Bordeynik‐Cohen, Mor
,
Birkan, Maria
,
Chang, Weise
,
Casadei, Silvia
,
Danial‐Farran, Nada
,
Abu‐Rayyan, Amal
,
Carlson, Ryan
,
Kamal, Lara
,
Arnthórsson, Asgeir Ö.
,
Sokolov, Meirav
,
Gilony, Dror
,
Lipschitz, Noga
,
Frydman, Moshe
,
Davidov, Bella
,
Macarov, Michal
,
Sagi, Michal
,
Vinkler, Chana
,
Poran, Hana
,
Sharony, Reuven
,
Samra, Nadra
,
Zvi, Na'ama
,
Baris‐Feldman, Hagit
,
Singer, Amihood
,
Handzel, Ophir
,
Hertzano, Ronna
,
Ali‐Naffaa, Doaa
,
Ruhrman‐Shahar, Noa
,
Madgar, Ory
,
Sofrin‐Drucker, Efrat
,
Peleg, Amir
,
Khayat, Morad
,
Shohat, Mordechai
,
Basel‐Salmon, Lina
,
Pras, Elon
,
Lev, Dorit
,
Wolf, Michael
,
Steingrimsson, Eirikur
,
Shomron, Noam
,
Kelley, Matthew W.
,
Kanaan, Moien N.
,
Allon‐Shalev, Stavit
,
King, Mary‐Claire
,
Avraham, Karen B.
Published in
Clinical genetics
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VENOUS THROMBOEMBOLISM, FACTOR V LEIDEN, AND METHYLENETETRAHYDROFOLATE REDUCTASE IN A SICKLE CELL ANEMIA PATIENT
by
Koren, Ariel
,
Zalman, Lucia
,
Levin, Carina
,
Hana, Manhal Abu
,
Mader, Rivka
,
Shalev, Stavit
Published in
Pediatric hematology and oncology
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The prenatal ultrasonic diagnosis of urethral obstruction and diverticulum of the urinary bladder
by
Shalev, J
,
Itzchak, Y
,
Blau, H
,
Rosenman, J
,
Ben Refael, Z
,
Brish, M
,
Mashiach, S
,
Serr, D M
Published in
Pediatric radiology
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