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European Journal of Pediatrics
|
April 1, 1989
Recurrent ascites in an infant with perinatally acquired cytomegalovirus infection
I Levy, M Shohat, Y Levy, et al.
AJNR. American Journal of Neuroradiology
|
November 1, 1988
CT of the temporal bone in achondroplasia
S 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 homogeneity
S Ash, C Johnson, M Shohat, et al.
Acta Paediatrica Scandinavica
|
March 1, 1984
Osmotic fragility of erythrocytes in newborn infants treated by phototherapy
G Alpert, M Shohat, S H Reisner, et al.
European Journal of Pediatrics
|
October 1, 1995
Aniridia: recent achievements in paediatric practice
I Ivanov, A Shuper, M Shohat, et al.
American Journal of Otolaryngology
|
February 9, 1999
Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G
M Shohat, N Fischel-Ghodsian, C Legum, et al.
Clinical Genetics
|
December 1, 1989
Autosomal dominant transmission of isolated congenital vertical talus
H J Stern, R D Clark, A J Stroberg, et al.
Critical Care Medicine
|
August 1, 1988
Determination of blood gases in children with extreme leukocytosis
M 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 origin
M 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 homogeneity
M Shohat, N Fischel-Ghodsian, J I Rotter, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 190) with videos related to
Sort By:
Page
of 19
European Journal of Pediatrics
|
April 1, 1989
Recurrent ascites in an infant with perinatally acquired cytomegalovirus infection
I Levy, M Shohat, Y Levy, et al.
AJNR. American Journal of Neuroradiology
|
November 1, 1988
CT of the temporal bone in achondroplasia
S 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 homogeneity
S Ash, C Johnson, M Shohat, et al.
Acta Paediatrica Scandinavica
|
March 1, 1984
Osmotic fragility of erythrocytes in newborn infants treated by phototherapy
G Alpert, M Shohat, S H Reisner, et al.
European Journal of Pediatrics
|
October 1, 1995
Aniridia: recent achievements in paediatric practice
I Ivanov, A Shuper, M Shohat, et al.
American Journal of Otolaryngology
|
February 9, 1999
Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G
M Shohat, N Fischel-Ghodsian, C Legum, et al.
Clinical Genetics
|
December 1, 1989
Autosomal dominant transmission of isolated congenital vertical talus
H J Stern, R D Clark, A J Stroberg, et al.
Critical Care Medicine
|
August 1, 1988
Determination of blood gases in children with extreme leukocytosis
M 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 origin
M 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 homogeneity
M Shohat, N Fischel-Ghodsian, J I Rotter, et al.
Page
of 19