High resolution computed tomography appearances of late sequelae of barium aspiration in an asymptomatic young child.
…, HA Rehman, A Abdul-Wahab - Saudi medical journal, 2005 - europepmc.org
Barium aspiration is a well-known complication of upper gastro-intestinal studies. Consequences
of aspiration are generally insignificant and leave no permanent changes in the lung …
of aspiration are generally insignificant and leave no permanent changes in the lung …
Pet ownership and associated respiratory diseases
Background Studies have shown that pets are very important sensitizing agents in patients
with asthma. Respiratory disorders and allergic diseases are common in the State of Qatar. …
with asthma. Respiratory disorders and allergic diseases are common in the State of Qatar. …
HRCT in cystic fibrosis in patients with CFTR I1234V mutation: assessment of scoring systems with low dose technique using multidetector system and correlation with …
Background and Aims: Pulmonary changes in patients with cystic fibrosis (CF) with CFTR
I1234V mutation have not been extensively documented. Impact of geographic influence on …
I1234V mutation have not been extensively documented. Impact of geographic influence on …
Antimicrobial resistance of bacterial strains isolated from respiratory tract of cystic fibrosis patients with CFTR I1234V mutation
SS Elshafie, AA Wahab… - Journal of Pediatric …, 2007 - thieme-connect.com
From the beginning of October 2002 until the end of April 2003, 72 samples from 36 cystic
fibrosis patients were examined in the Microbiology Laboratory, Hamad Medical Corporation. …
fibrosis patients were examined in the Microbiology Laboratory, Hamad Medical Corporation. …
Sandhoff disease (GM2 gangliosidoses) in a premature patient with bronchopulmonary dysplasia
A Abdul-Wahab, MS Bessisso, MF Elsaid - Neurosciences Journal, 2002 - nsj.org.sa
We report a female premature infant with bronchopulmonary dysplasia and Sandhoff disease.
The clue for diagnosis was the fundoscopy examination. We discuss this rare disease with …
The clue for diagnosis was the fundoscopy examination. We discuss this rare disease with …
[CITATION][C] The incidence patterns of Down syndrome in Qatar
AA Wahab, A Bener, AS Teebi - Clinical genetics, 2006 - Wiley Online Library
Down syndrome (DS) incidence ranges from 0.3 to 3.4 per 1000 births in different parts of the
world and is generally thought to be around 1: 1000 births in Europe and North America (1–…
world and is generally thought to be around 1: 1000 births in Europe and North America (1–…
[PDF][PDF] Chest radIoloGy
Background and Aims: Pulmonary changes in patients with cystic fibrosis (CF) with CFTR
I1234V mutation have not been extensively documented. Impact of geographic inluence on …
I1234V mutation have not been extensively documented. Impact of geographic inluence on …
Cystic fibrosis in a child from Syria
AA Wahab, IA Janahi, S Hebi, M Al-Hamed… - Annals of tropical …, 2002 - Taylor & Francis
We describe a Syrian child with typical features of severe cystic fibrosis (CF) phenotype and
a positive sweat test. DNA analysis confirmed homozygosity for the Δ F508 mutation on …
a positive sweat test. DNA analysis confirmed homozygosity for the Δ F508 mutation on …
Evolution and sequelae of acquired lobar emphysema in a premature infant with chronic lung disease
V Bhat, AW Atiqa - 2004 - pesquisa.bvsalud.org
The evolution of acquired lobar emphysema in a premature infant with chronic pulmonary
disease was demonstrated by serial radiological examinations using multiple imaging …
disease was demonstrated by serial radiological examinations using multiple imaging …
[CITATION][C] Baseline exhaled nitric oxide level in cystic fibrosis patients with I1234V mutation is lower than normal and affected by gender and airway microbiome
METHODS: All patients with confirmed homozygous I1234V CFTR mutation in Hamad
Medical Corporation CF center were enrolled in the study. Portable nitric oxide analyzer (NIOX …
Medical Corporation CF center were enrolled in the study. Portable nitric oxide analyzer (NIOX …
