Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N Sakati

Showing results (11-20 of 36) with videos related to

Pageof 4
Sort By:
The Journal of Pediatrics|January 1, 1978
Atypical ichthyosiform erythroderma and congenital neurosensory deafness--a distinct syndromeT P Senter, K L Jones, N Sakati, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 1, 1987
The multiple manifestations of the encephalocraniocutaneous lipomatosis syndromeO Al-Mefty, J L Fox, N Sakati, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1996
A novel mutation in the deoxyribonucleic acid-binding domain of the vitamin D receptor causes hereditary 1,25-dihydroxyvitamin D-resistant ricketsN U Lin, P J Malloy, N Sakati, et al.
European Journal of Pediatrics|January 1, 1989
Cystic fibrosis in Saudi ArabiaH Nazer, E Riff, N Sakati, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric proteinJ D Cogan, J A Phillips, S S Schenkman, et al.
Clinical Genetics|June 1, 1985
Multiple dysmorphic features and pancytopenia: a new syndrome?K Sackey, N Sakati, R J Aur, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1993
Heterogeneous growth hormone (GH) gene mutations in familial GH deficiencyJ D Cogan, J A Phillips, N Sakati, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 23, 2001
Endocrine sequelae of childhood craniopharyngiomaB Bin-Abbas, H Mawlawi, N Sakati, et al.
Neurosurgery|October 1, 1985
Microsurgery for giant craniopharyngiomas in childrenO Al-Mefty, M Hassounah, P Weaver, et al.
Clinical and Experimental Rheumatology|September 22, 2005
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among ArabsS M Al-Mayouf, A AlMehaidib, S Bahabri, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
The Journal of Pediatrics|January 1, 1978
Atypical ichthyosiform erythroderma and congenital neurosensory deafness--a distinct syndromeT P Senter, K L Jones, N Sakati, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 1, 1987
The multiple manifestations of the encephalocraniocutaneous lipomatosis syndromeO Al-Mefty, J L Fox, N Sakati, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1996
A novel mutation in the deoxyribonucleic acid-binding domain of the vitamin D receptor causes hereditary 1,25-dihydroxyvitamin D-resistant ricketsN U Lin, P J Malloy, N Sakati, et al.
European Journal of Pediatrics|January 1, 1989
Cystic fibrosis in Saudi ArabiaH Nazer, E Riff, N Sakati, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric proteinJ D Cogan, J A Phillips, S S Schenkman, et al.
Clinical Genetics|June 1, 1985
Multiple dysmorphic features and pancytopenia: a new syndrome?K Sackey, N Sakati, R J Aur, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1993
Heterogeneous growth hormone (GH) gene mutations in familial GH deficiencyJ D Cogan, J A Phillips, N Sakati, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 23, 2001
Endocrine sequelae of childhood craniopharyngiomaB Bin-Abbas, H Mawlawi, N Sakati, et al.
Neurosurgery|October 1, 1985
Microsurgery for giant craniopharyngiomas in childrenO Al-Mefty, M Hassounah, P Weaver, et al.
Clinical and Experimental Rheumatology|September 22, 2005
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among ArabsS M Al-Mayouf, A AlMehaidib, S Bahabri, et al.
Pageof 4