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H Shalev

Showing results (21-30 of 44) with videos related to

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Pediatric Hematology and Oncology|April 1, 1999
No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type IH Tamary, H Shalev, V Pinsk, et al.
Archives of Disease in Childhood|May 14, 1998
Clinical presentation and outcome in primary familial hypomagnesaemiaH Shalev, M Phillip, A Galil, et al.
American Journal of Human Genetics|October 30, 1998
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mappingN B Haider, R Carmi, H Shalev, et al.
Pediatric Nephrology (Berlin, Germany)|April 25, 2000
Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney diseaseD Landau, H Shalev, H Shulman, et al.
The Journal of Pediatrics|March 10, 2001
Familial hemolytic uremic syndrome associated with complement factor H deficiencyD Landau, H Shalev, G Levy-Finer, et al.
Hepatology (Baltimore, Md.)|September 1, 1988
Extent of measles hepatitis in various agesH Shalev-Zimels, Z Weizman, C Lotan, et al.
The Journal of Pediatrics|February 7, 2001
Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newbornH Shalev, A Moser, J Kapelushnik, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 6, 2021
Associations between breast implants and postpartum lactational mastitis in breastfeeding women: retrospective studyH Shalev Ram, S Ram, I Wiser, et al.
Molecular Genetics and Metabolism|June 3, 2004
A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindredD Landau, D Cohen, H Shalev, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Erythropoietin deficiency causes anemia in nephrotic children with normal kidney functionS Feinstein, R Becker-Cohen, N Algur, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Pediatric Hematology and Oncology|April 1, 1999
No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type IH Tamary, H Shalev, V Pinsk, et al.
Archives of Disease in Childhood|May 14, 1998
Clinical presentation and outcome in primary familial hypomagnesaemiaH Shalev, M Phillip, A Galil, et al.
American Journal of Human Genetics|October 30, 1998
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mappingN B Haider, R Carmi, H Shalev, et al.
Pediatric Nephrology (Berlin, Germany)|April 25, 2000
Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney diseaseD Landau, H Shalev, H Shulman, et al.
The Journal of Pediatrics|March 10, 2001
Familial hemolytic uremic syndrome associated with complement factor H deficiencyD Landau, H Shalev, G Levy-Finer, et al.
Hepatology (Baltimore, Md.)|September 1, 1988
Extent of measles hepatitis in various agesH Shalev-Zimels, Z Weizman, C Lotan, et al.
The Journal of Pediatrics|February 7, 2001
Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newbornH Shalev, A Moser, J Kapelushnik, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 6, 2021
Associations between breast implants and postpartum lactational mastitis in breastfeeding women: retrospective studyH Shalev Ram, S Ram, I Wiser, et al.
Molecular Genetics and Metabolism|June 3, 2004
A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindredD Landau, D Cohen, H Shalev, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 29, 2001
Erythropoietin deficiency causes anemia in nephrotic children with normal kidney functionS Feinstein, R Becker-Cohen, N Algur, et al.
Pageof 5