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M Shohat

Showing results (81-90 of 190) with videos related to

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European Journal of Pediatrics|April 1, 1989
Recurrent ascites in an infant with perinatally acquired cytomegalovirus infectionI Levy, M Shohat, Y Levy, et al.
AJNR. American Journal of Neuroradiology|November 1, 1988
CT of the temporal bone in achondroplasiaS R Cobb, M Shohat, C M Mehringer, et al.
Israel Journal of Medical Sciences|August 1, 1994
Further mapping of the properdin deficiency gene in a Tunisian Jewish family--evidence for genetic homogeneityS Ash, C Johnson, M Shohat, et al.
Acta Paediatrica Scandinavica|March 1, 1984
Osmotic fragility of erythrocytes in newborn infants treated by phototherapyG Alpert, M Shohat, S H Reisner, et al.
European Journal of Pediatrics|October 1, 1995
Aniridia: recent achievements in paediatric practiceI Ivanov, A Shuper, M Shohat, et al.
American Journal of Otolaryngology|February 9, 1999
Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555GM Shohat, N Fischel-Ghodsian, C Legum, et al.
Clinical Genetics|December 1, 1989
Autosomal dominant transmission of isolated congenital vertical talusH J Stern, R D Clark, A J Stroberg, et al.
Critical Care Medicine|August 1, 1988
Determination of blood gases in children with extreme leukocytosisM Shohat, T Schonfeld, R Zaizoz, et al.
American Journal of Public Health|May 1, 1989
Hypertension in Israeli adolescents: prevalence according to weight, sex and parental originM Shohat, T Shohat, M Mimouni, et al.
Advances in Experimental Medicine and Biology|January 1, 1995
The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneityM Shohat, N Fischel-Ghodsian, J I Rotter, et al.
Pageof 19

Showing results (81-90 of 190) with videos related to

Sort By:
Pageof 19
European Journal of Pediatrics|April 1, 1989
Recurrent ascites in an infant with perinatally acquired cytomegalovirus infectionI Levy, M Shohat, Y Levy, et al.
AJNR. American Journal of Neuroradiology|November 1, 1988
CT of the temporal bone in achondroplasiaS R Cobb, M Shohat, C M Mehringer, et al.
Israel Journal of Medical Sciences|August 1, 1994
Further mapping of the properdin deficiency gene in a Tunisian Jewish family--evidence for genetic homogeneityS Ash, C Johnson, M Shohat, et al.
Acta Paediatrica Scandinavica|March 1, 1984
Osmotic fragility of erythrocytes in newborn infants treated by phototherapyG Alpert, M Shohat, S H Reisner, et al.
European Journal of Pediatrics|October 1, 1995
Aniridia: recent achievements in paediatric practiceI Ivanov, A Shuper, M Shohat, et al.
American Journal of Otolaryngology|February 9, 1999
Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555GM Shohat, N Fischel-Ghodsian, C Legum, et al.
Clinical Genetics|December 1, 1989
Autosomal dominant transmission of isolated congenital vertical talusH J Stern, R D Clark, A J Stroberg, et al.
Critical Care Medicine|August 1, 1988
Determination of blood gases in children with extreme leukocytosisM Shohat, T Schonfeld, R Zaizoz, et al.
American Journal of Public Health|May 1, 1989
Hypertension in Israeli adolescents: prevalence according to weight, sex and parental originM Shohat, T Shohat, M Mimouni, et al.
Advances in Experimental Medicine and Biology|January 1, 1995
The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneityM Shohat, N Fischel-Ghodsian, J I Rotter, et al.
Pageof 19