Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Allie Moosa"'
Publikováno v:
Cell Biochemistry and Function. 22:365-371
Peroxisomes, also termed as microbodies, are now known to carry out several specialized metabolic activities that are vital to cellular function. A defect in peroxisomal function leads to development of a fatal human disease, and a number of peroxiso
Autor:
Yasuhiro Indo, Essam A.R. Ismail, Generoso Andria, Sek Mardy, Ichiro Matsuda, Gail E. Graham, Philippe M. Frossard, László Sztriha, Fumio Endo, Alfons Macaya, Yuichi Miura, William T. Gibson, Ennio Toscano, Allie Moosa
Publikováno v:
The American Journal of Human Genetics. 64(6):1570-1579
SummaryCongenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of unexplained fever, anhidrosis (inability to sweat), absence of reaction to noxious stimuli, self-mutilating behavior, and mental retardation. Hum
Publikováno v:
Journal of Child Neurology. 13:243-246
Autor:
Allie Moosa, Mohammad Z. Haider
Publikováno v:
Journal of Child Neurology. 12:310-313
Spinal muscular atrophy is an autosomal recessive disorder characterized by degeneration of lower motor neurons. We have investigated the presence of survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletions in 17 Arab and 1
Publikováno v:
Medical Teacher. 17:289-296
Medical schools use a variety of methods to assess the clinical competence of students. The aim of this study was to evaluate the system in use at the Department of Paediatrics at Kuwait University. The analysis of the performance of 142 second clini
Publikováno v:
Pediatric Nephrology. 8:205-210
Progressive encephalopathy, developmental delay, microcephaly, electroencephalogram (EEG) and computed tomographic (CT) scan abnormalities have been reported in 80% of children with chronic renal failure (CRF) in infancy. Malnutrition, aluminium into
Publikováno v:
Journal of child neurology. 21(5)
The congenital muscular dystrophies are autosomal recessive disorders with different clinical phenotypes, the spectrum of which varies between different ethnic communities. We report our findings in 21 Arab children with congenital muscular dystrophy
Publikováno v:
Annals of Saudi Medicine. 15:209-211
Splenomegaly was found in 31 (55%) of 56 Arab children with idiopathic thrombocytopenic purpura. Of those with splenomegaly, 84% had evidence of iron deficiency anemia compared to 48% in those without splenomegaly (P0.001). There was no significant d
Autor:
Allie Moosa, Mustafa Kadri
Publikováno v:
Medical Principles and Practice. 4:114-116
Three brands of commercial honey were tested for their inhibitory effect on the growth of Helicobαcter pylori. H. pylori were isolated from gastric mucosa biopsy specimens using bot
Autor:
Allie Moosa, Renu Gupta, M. Al-Bloushi, Adekunle Adekile, F. Yacoub, Y. Habeeb, T. Sinan, Mohammad Z. Haider
Publikováno v:
American journal of hematology. 70(3)
Overt stroke is rare among sickle cell disease (SCD) patients in Kuwait. However, there are no previous studies of silent cerebral infarcts, which have been described in up to 20% of American children with Hb SS. We have carried out a prospective bra