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Hormone Research
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January 1, 1986
Hereditary resistance to 1,25-dihydroxyvitamin D: clinical and radiological improvement during high-dose oral calcium therapy
N Sakati, N J Woodhouse, N Niles, et al.
American Journal of Medical Genetics
|
July 1, 1983
The Börjeson-Forssman-Lehmann syndrome
L K Robinson, K L Jones, F Culler, et al.
Journal of Pediatric Surgery
|
August 1, 1995
Persistent hyperinsulinemic hypoglycemia of infancy: experience with 28 cases
A al-Rabeeah, A al-Ashwal, A al-Herbish, et al.
Journal of Child Neurology
|
April 1, 1992
Saudi variant of multiple sulfatase deficiency
A al Aqeel, P T Ozand, J Brismar, et al.
The Western Journal of Medicine
|
January 1, 1976
Genetic counseling. An evaluation of public health genetic clinics
K J Reid, N Sakati, L L Prichard, et al.
American Journal of Medical Genetics
|
June 22, 1999
Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement
G A Diaz, B D Gelb, F Ali, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 24, 1998
Different faces of non-autoimmune diabetes of infancy
N Attia, A Zahrani, R Saif, et al.
Annals of Saudi Medicine
|
March 8, 2007
Wolman's disease: The King Faisal Specialist Hospital and Research Centre experience
M Al Essa, R Nounou, N Sakati, et al.
Annals of Saudi Medicine
|
November 1, 1994
Syndrome of camptodactyly, arthropathy and coxa vara (CAC syndrome)
S Bahabri, N Sakati, C Hugosson, et al.
Journal of Pediatric Hematology/Oncology
|
November 1, 1995
Bone marrow transplantation for infantile malignant osteopetrosis
H Solh, A M Da Cunha, N Giri, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
Hormone Research
|
January 1, 1986
Hereditary resistance to 1,25-dihydroxyvitamin D: clinical and radiological improvement during high-dose oral calcium therapy
N Sakati, N J Woodhouse, N Niles, et al.
American Journal of Medical Genetics
|
July 1, 1983
The Börjeson-Forssman-Lehmann syndrome
L K Robinson, K L Jones, F Culler, et al.
Journal of Pediatric Surgery
|
August 1, 1995
Persistent hyperinsulinemic hypoglycemia of infancy: experience with 28 cases
A al-Rabeeah, A al-Ashwal, A al-Herbish, et al.
Journal of Child Neurology
|
April 1, 1992
Saudi variant of multiple sulfatase deficiency
A al Aqeel, P T Ozand, J Brismar, et al.
The Western Journal of Medicine
|
January 1, 1976
Genetic counseling. An evaluation of public health genetic clinics
K J Reid, N Sakati, L L Prichard, et al.
American Journal of Medical Genetics
|
June 22, 1999
Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement
G A Diaz, B D Gelb, F Ali, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 24, 1998
Different faces of non-autoimmune diabetes of infancy
N Attia, A Zahrani, R Saif, et al.
Annals of Saudi Medicine
|
March 8, 2007
Wolman's disease: The King Faisal Specialist Hospital and Research Centre experience
M Al Essa, R Nounou, N Sakati, et al.
Annals of Saudi Medicine
|
November 1, 1994
Syndrome of camptodactyly, arthropathy and coxa vara (CAC syndrome)
S Bahabri, N Sakati, C Hugosson, et al.
Journal of Pediatric Hematology/Oncology
|
November 1, 1995
Bone marrow transplantation for infantile malignant osteopetrosis
H Solh, A M Da Cunha, N Giri, et al.
Page
of 4