[HTML][HTML] Awareness regarding childhood asthma in Saudi Arabia
…, A Al-Khorayyef, M Al-Qwaiee… - Annals of Thoracic …, 2016 - journals.lww.com
OBJECTIVE: Assessing the knowledge and awareness of the Saudi society about bronchial
asthma in children. METHODS: Structured questionnaires were randomly distributed to …
asthma in children. METHODS: Structured questionnaires were randomly distributed to …
[HTML][HTML] Prevalence of obstructive sleep apnea in children with sickle cell disease at a tertiary hospital in Saudi Arabia
T Al-Otaibi, M Al-Qwaiee, H Faraidi, F Batniji… - Saudi Medical …, 2017 - ncbi.nlm.nih.gov
Objectives: To assess the prevalence of obstructive sleep apnea in Saudi children with
sickle cell disease at a tertiary hospital in Kingdom of Saudi Arabia (KSA) using nocturnal …
sickle cell disease at a tertiary hospital in Kingdom of Saudi Arabia (KSA) using nocturnal …
[HTML][HTML] Severe asthma in children: An official statement from Saudi Pediatric Pulmonology Association
…, SA Alharbi, TM Almaghamsi, MM Al Qwaiee… - Saudi Medical …, 2022 - ncbi.nlm.nih.gov
In Saudi Arabia, the prevalence of pediatric asthma ranges between 8% and 25%. However,
there are no sufficient data regarding severe asthma in childhood in Saudi Arabia. …
there are no sufficient data regarding severe asthma in childhood in Saudi Arabia. …
Genotype and phenotype of adenosine deaminase 2 deficiency: a report from Saudi Arabia
…, F Albatniji, H Alfaraidi, TB Ali, M Al Qwaiee… - Journal of Clinical …, 2023 - Springer
Adenosine deaminase 2 deficiency (DADA2), a rare and potentially fatal systemic
autoinflammatory disease, is characterized by low or lack of ADA2 activity due to ADA2 mutations. …
autoinflammatory disease, is characterized by low or lack of ADA2 activity due to ADA2 mutations. …
[HTML][HTML] An Infant Presenting with Interstitial Lung Disease Diagnosed Later as Hunter Syndrome: A Case Report
B AlTami, H AlKelabi, MM Al-Qwaiee - The American Journal of …, 2022 - ncbi.nlm.nih.gov
Objective: Unusual clinical course Background: Hunter syndrome is a multisystem metabolic
inherited disease belonging to the large group of mucopolysaccharidoses (MPSs). Hunter …
inherited disease belonging to the large group of mucopolysaccharidoses (MPSs). Hunter …
Genotype and Phenotype of Adenosine Deaminase 2 Deficiency: The Experience From Saudi Arabia
…, F Albatniji, H Alfaraidi, TB Ali, M Al Qwaiee… - 2022 - researchsquare.com
Purpose DADA2 is a rare and potentially fatal systemic autoinflammatory disease characterized
by reduced or absence of ADA2 enzyme activity resulting from mutations in the ADA2 …
by reduced or absence of ADA2 enzyme activity resulting from mutations in the ADA2 …
Severe tracheomalacia secondary to double aortic arch. Any role in posterior aortopexy? A case report
AM Bayan, AQ Mansour, AE Ayed, B Khaled, A Otay… - 2018 - pesquisa.bvsalud.org
Tracheomalacia is the abnormal collapse of the tracheal lumen and is common after cardiac
compression. In the severe types, tracheomalacia can lead to significant morbidity, …
compression. In the severe types, tracheomalacia can lead to significant morbidity, …