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

H El-Shanti

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Acta Haematologica|June 3, 1999
Effect of desferrioxamine in acute haemolytic anaemia of glucose-6-phosphate dehydrogenase deficiencyH S al-Rimawi, M al-Sheyyab, A Batieha, et al.
The Journal of Pediatrics|September 1, 1993
Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetateP P Tóth, H el-Shanti, S Eivins, et al.
European Journal of Pediatrics|January 25, 2002
The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a reviewH A Majeed, M Al-Tarawna, H El-Shanti, et al.
European Journal of Pediatrics|December 29, 2000
Familial disorder of sex determination in seven individuals from three related sibshipsN Jarrah, H El-Shanti, A Khier, et al.
American Journal of Human Genetics|September 1, 1995
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical regionA J Mears, H el-Shanti, J C Murray, et al.
QJM : Monthly Journal of the Association of Physicians|January 5, 2000
Familial Mediterranean fever in children: the expanded clinical profileH A Majeed, M Rawashdeh, H el-Shanti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate geneH el-Shanti, J C Murray, E V Semina, et al.
Journal of Tropical Pediatrics|October 1, 1996
Neonatal meningitis in northern JordanA S Daoud, M al-Sheyyab, F Abu-Ekteish, et al.
European Journal of Pediatrics|April 25, 2001
Bleeding tendency in Wolfram syndrome: a newly identified feature with phenotype genotype correlationM al-Sheyyab, N Jarrah, E Younis, et al.
American Journal of Human Genetics|March 20, 2001
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3K Wang, E W Pugh, S Griffen, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Acta Haematologica|June 3, 1999
Effect of desferrioxamine in acute haemolytic anaemia of glucose-6-phosphate dehydrogenase deficiencyH S al-Rimawi, M al-Sheyyab, A Batieha, et al.
The Journal of Pediatrics|September 1, 1993
Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetateP P Tóth, H el-Shanti, S Eivins, et al.
European Journal of Pediatrics|January 25, 2002
The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a reviewH A Majeed, M Al-Tarawna, H El-Shanti, et al.
European Journal of Pediatrics|December 29, 2000
Familial disorder of sex determination in seven individuals from three related sibshipsN Jarrah, H El-Shanti, A Khier, et al.
American Journal of Human Genetics|September 1, 1995
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical regionA J Mears, H el-Shanti, J C Murray, et al.
QJM : Monthly Journal of the Association of Physicians|January 5, 2000
Familial Mediterranean fever in children: the expanded clinical profileH A Majeed, M Rawashdeh, H el-Shanti, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate geneH el-Shanti, J C Murray, E V Semina, et al.
Journal of Tropical Pediatrics|October 1, 1996
Neonatal meningitis in northern JordanA S Daoud, M al-Sheyyab, F Abu-Ekteish, et al.
European Journal of Pediatrics|April 25, 2001
Bleeding tendency in Wolfram syndrome: a newly identified feature with phenotype genotype correlationM al-Sheyyab, N Jarrah, E Younis, et al.
American Journal of Human Genetics|March 20, 2001
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3K Wang, E W Pugh, S Griffen, et al.
Pageof 3