Authors:
Haider, MZ
Devarajan, LV
Al-Essa, M
Srivastva, BS
Kumar, H
Azad, R
Rashwan, N
Citation: Mz. Haider et al., Retinopathy of prematurity: Mutations in the Norrie disease gene and the risk of progression to advanced stages, PEDIATR INT, 43(2), 2001, pp. 120-123
Authors:
Haider, MZ
Moosa, A
Dalal, H
Habib, Y
Reynold, L
Citation: Mz. Haider et al., Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes, J BIOMED SC, 8(2), 2001, pp. 191-196
Authors:
Adekile, AD
Kutlar, F
Haider, MZ
Kutlar, A
Citation: Ad. Adekile et al., Frequency of the 677 C -> T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients, AM J HEMAT, 66(4), 2001, pp. 263-266
Citation: Z. Hijazi et Mz. Haider, Influence of consanguinity and IgE receptor genotypes on clinical manifestations of asthma in Kuwaiti children, J TROP PEDI, 47(1), 2001, pp. 13-16
Citation: A. Al-eisa et al., Angiotensin converting enzyme gene insertion/deletion polymorphism in idiopathic nephrotic syndrome in Kuwaiti Arab children, SC J UROL N, 35(3), 2001, pp. 239-242
Authors:
Adekile, AD
Gupta, R
Yacoub, F
Sinan, T
Al-Bloushi, M
Haider, MZ
Citation: Ad. Adekile et al., Avascular necrosis of the hip in children with sickle cell disease and high Hb F: Magnetic resonance imaging findings and influence of alpha-thalassemia trait, ACT HAEMAT, 105(1), 2001, pp. 27-31
Citation: A. Al-eisa et al., Angiotensin-converting enzyme gene insertion/deletion polymorphism and renal damage in childhood uropathies, PEDIATR INT, 42(4), 2000, pp. 348-353
Citation: Z. Hijazi et Mz. Haider, Interleukin-4 gene promoter polymorphism [C590T] and asthma in Kuwaiti Arabs, INT A AL IM, 122(3), 2000, pp. 190-194
Authors:
Raghupathy, R
Haider, MZ
Azizieh, F
D'Souza, TM
Abdelsalam, R
Adekile, AD
Citation: R. Raghupathy et al., Tumor necrosis factor-alpha is undetectable in the plasma of SS patients with elevated Hb F, AM J HEMAT, 64(2), 2000, pp. 91-94
Authors:
Haider, MZ
Devarajan, LV
Al-Essa, M
Srivastva, BS
Kumar, H
Azad, R
Rashwan, N
Citation: Mz. Haider et al., Missense mutations in Norrie disease gene are not associated with advancedstages of retinopathy of prematurity in Kuwaiti Arabs, BIOL NEONAT, 77(2), 2000, pp. 88-91
Authors:
Diejomaoh, FME
Haider, MZ
Dalal, H
Abdulaziz, A
D'Souza, TM
Adekile, AD
Citation: Fme. Diejomaoh et al., Influence of alpha-thalassemia trait on the prevalence and severity of anemia in pregnancy among women in Kuwait, ACT HAEMAT, 104(2-3), 2000, pp. 92-94
Authors:
Haider, MZ
Shaltout, A
Alsaeid, K
Al-Khawari, M
Dorman, JS
Citation: Mz. Haider et al., High frequency of HLA-DQB1 non-Asp(57) alleles in Kuwaiti children with insulin-dependent diabetes mellitus, HUMAN HERED, 50(4), 2000, pp. 242-246
Citation: Mz. Haider et Z. Hijazi, Prevalence of angiotensin converting enzyme gene insertion/deletion polymorphism in Kuwaiti Arabs with asthma, MED SCI RES, 27(8), 1999, pp. 553-556
Authors:
Haider, MZ
Shaltout, A
Alsaeid, K
Qabazard, M
Dorman, J
Citation: Mz. Haider et al., Prevalence of human leukocyte antigen DQA1 and DQB1 alleles in Kuwaiti Arab children with type 1 diabetes mellitus, CLIN GENET, 56(6), 1999, pp. 450-456