Výsledky vyhledávání - "Q. A. Al-Saleh"

Autor: Q A al Saleh, A I Rostom, N M Najem, A S al-Fouzan

Publikováno v: International Journal of Dermatology. 30:519-521

Twenty-four patients suffering from single or multiple lesions of cutaneous leishmaniasis were included in this study. Most of the lesions were on the extremities. The patients were randomly divided into two groups. Most of the patients in the first

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753934de39c4961b6b0f858ab36a3d2a
https://doi.org/10.1111/j.1365-4362.1991.tb04878.x

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Bone marrow examination in childhood idiopathic thrombocytopenic purpura: Is it routinely indicated?

Autor: Omar H, Helmy A. Qurtom, Aboel-Hassan Hm, M. M. Lubani, Q A al-Saleh

Publikováno v: Annals of Saudi medicine. 12(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5910fe6699acca700d91ee32c18cd98
https://pubmed.ncbi.nlm.nih.gov/17589171

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Cystic fibrosis and Helicobacter pylori gastritis, megaloblastic anaemia, subnormal mentality and minor anomalies in two siblings: a new syndrome?

Autor: M. M. Lubani, A. S. Teebi, Q. A. Al-Saleh, A. Moosa, M. H. Kalaoui

Publikováno v: European journal of pediatrics. 150(4)

Two siblings of consanguineous Arab parents were found to have cystic fibrosis and gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anaemia, subnormal mentality and minor anomalies. The association of H. pylori and megal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f192f06b789a424de97dfb20a02bfbd
https://pubmed.ncbi.nlm.nih.gov/2029916

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Successful pregnancies following remission in childhood acute lymphoblastic leukaemia--case report

Autor: A. A. Al-Rashied, K. C. Aboo-Backer, H. S. Al-Rimawi, Q. A. Al-Saleh, S. Malik, M. F. Jallad

Publikováno v: Annals of tropical paediatrics. 11(3)

SummaryWe report two successful pregnancies in a 17-year-old Arab girl who had received modern combination chemotherapy and central nervous system minimal disease therapy for childhood acute lymphoblastic leukaemia at the age of 9.5 years.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8a54fa820e5729754df0794ae42bc93
https://pubmed.ncbi.nlm.nih.gov/1719933

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Prevalence of congenital adrenal hyperplasia in Kuwait

Autor: Y. K. Abdul Al, K I Dudin, P. C. Reavey, A. R. A. Issa, Ahmad S. Teebi, R. Bushnaq, E. A. R. Ismail, Q. A. Al-Saleh, D.S. Manandhar, M.Y. El-Khalifa, M. M. Lubani

Publikováno v: European Journal of Pediatrics. 149:391-392

Between 1978 and 1988 congenital adrenal hyperplasia (CAH) was diagnosed in 60 children in Kuwait with an estimated prevalence of 1:9,000 livebirths, which is higher than that reported from Europe and Canada. In addition, there was presumptive eviden

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353dfbfdb09945e6c2478fb6107fc83f
https://doi.org/10.1007/bf02009655

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Vitamin-D-deficiency rickets in Kuwait: the prevalence of a preventable disease

Autor: M. A. A. Moussa, M. M. Lubani, Q. A. Al-Saleh, P. C. Reavey, S.A.H. Ahmed, S.A. Quattawi, D. C. Sharda, T. S. Al-Shab

Publikováno v: Annals of Tropical Paediatrics. 9:134-139

Two hundred and fifty children with clinical, biochemical and radiological evidence of vitamin-D-deficiency rickets were studied over a period of 5 years. Their ages ranged from 1 month to 2 years. Breastfed infants formed 63% of total cases. Intramu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e44320e77581c6d639ef8a3b0a586b1a
https://doi.org/10.1080/02724936.1989.11748616

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Congenital Hypothyroidism in Kuwait

Autor: Q. A. Al-Saleh, A. S. Teebi, M. Zaki, Azhar S. Daoud, S. A. Al-Awadi

Publikováno v: Journal of Tropical Pediatrics. 35:312-314

During a 7-year period (1981-1987), 25 children with congenital hypothyroidism were diagnosed in a regional hospital in Kuwait. The calculated incidence was 1:3476 live births. The diagnosis relied on clinical manifestation and confirmed by thyroid f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f66911fc55fbde08ba2899bc50480b45
https://doi.org/10.1093/tropej/35.6.312

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The value of red cell distribution width in the diagnosis of anaemia in children

Autor: N Kaddoorah, H A Qurtom, A Hassanein, M A Qurtom, M. M. Lubani, Q A al-Saleh, T al-Sheikh

Publikováno v: European journal of pediatrics. 148(8)

The red cell distribution width index (RDW) was determined in 103 normal children, 69 iron-deficient (ID) patients, 73 with the thalassaemia trait, and 71 with other haemoglobinopathies. Elevated RDW values were found in anaemic patients, the highest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c6971695421766c81b88fe8186b5882
https://pubmed.ncbi.nlm.nih.gov/2792125

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New autosomal recessive faciodigitogenital syndrome

Autor: Q. A. Al-Saleh, Sadika A. Al-Awadi, Ahmad S. Teebi, K.K. Naguib

Most pedigrees of Aarskog's faciodigitogenital syndrome have suggested X linked inheritance. However, sex influenced autosomal dominant inheritance is also a possibility in some families. We describe an Arab family of normal consanguineous parents wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab121d3f60bc62a062b3e4fd890b1db2
https://europepmc.org/articles/PMC1050509/

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