Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Amal Al-Naimi"'
Autor:
Ahmed Abushahin, Amal Al-Naimi, Mutasim Abu-Hasan, Rania Arar, M. Lina Hayati, Antonisamy Belavendra, Ibrahim A. Janahi
Publikováno v:
Canadian Respiratory Journal, Vol 2023 (2023)
Introduction. Sleep-disordered breathing (SDB) is common in patients with Prader–Willi Syndrome (PWS). However, the prevalence of SDB varies widely between studies. Early identification of SDB and factors contributing to its incidence is essential,
Externí odkaz:
https://doaj.org/article/b991246ed8e74628a9df657254e2e233
Publikováno v:
Pulmonary Medicine, Vol 2022 (2022)
Introduction/Purpose. Tracheoesophageal fistula (TEF) represents one of the most common congenital developmental malformations of the upper digestive tract. The optimal surgical management has several controversies, particularly in rapidly developing
Externí odkaz:
https://doaj.org/article/c506303458eb4fac8fe84f77aa2646b5
Publikováno v:
Case Reports in Genetics, Vol 2022 (2022)
Farber disease (FD) is an extremely rare autosomal recessive disorder caused by the deficiency of lysosomal acid ceramidase. It is characterized by a triad of progressive multiple joints’ involvement, subcutaneous nodules, and hoarseness of voice.
Externí odkaz:
https://doaj.org/article/1ab6aecbb52142f9b4ae72bea3b2cf29
Publikováno v:
Case Reports in Pulmonology, Vol 2021 (2021)
Pleuropulmonary blastoma (PPB) is a rare intrathoracic malignancy, which arises from the lung parenchyma and/or pleura. PPB has strong genetic association with mutations in DICER1 gene. Despite being rare, PPB is the most common lung tumor in childre
Externí odkaz:
https://doaj.org/article/19f2607042704f84b5d4aa5361dc0374
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 30, Iss C, Pp 25-27 (2018)
Pediatric germ cell tumors (GCT) rarely occur in the head and neck region and they are rarely associated with congenital anomalies. A 17 month old girl presented with a history of cough and change in voice for one month. Her chest x-ray and cross sec
Externí odkaz:
https://doaj.org/article/45f60597d2d2467f8ea7fac7d6edf6ba
Publikováno v:
Case Reports in Pulmonology
Case Reports in Pulmonology, Vol 2021 (2021)
Case Reports in Pulmonology, Vol 2021 (2021)
Pleuropulmonary blastoma (PPB) is a rare intrathoracic malignancy, which arises from the lung parenchyma and/or pleura. PPB has strong genetic association with mutations in DICER1 gene. Despite being rare, PPB is the most common lung tumor in childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a91d8667f976d15488c0fe6ae50f502
https://doi.org/10.1155/2021/1983864
https://doi.org/10.1155/2021/1983864
Publikováno v:
Qatar Medical Journal
We report two cases of Qatari children with cystic fibrosis (CF) from different families presenting the homozygous CFTR 1521_1523delCTT (p. Phe508del) mutation with classic CF phenotypes. This gene mutation is considered the second CF mutation identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e28335241a118781a5d018225efa0b
http://europepmc.org/articles/PMC8314207
http://europepmc.org/articles/PMC8314207
Publikováno v:
Cureus
Background and objectives Tracheal bronchus (TB) is a rare congenital airway anomaly originating from the trachea, with a reported prevalence of 0.9%-3% in children. Although TB was studied in the literature, this anomaly was not evaluated in Qatar.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdc3af891e6a9f011d0ef760278d9802
http://europepmc.org/articles/PMC8221636
http://europepmc.org/articles/PMC8221636
Autor:
Khalid A. Fakhro, Fatima Al Ali, Mehdi Adeli, Salim Bougarn, Alya Al-Shakaki, Amel Hassan, Debra O. Prosser, Eman Al Maslamani, Rafah Mackeh, Donald R. Love, Amal Al-Naimi, Taushif Khan, Manar Ata, Mohammed Yousuf Karim, Ronald G. Crystal, Bernice Lo, Waleed Aamer, Nico Marr, Khawla Al-Darwish, Ibrahim A. Janahi, Qian Zhang, Amjad Tuffaha, Mahbuba Rahman, Tanwir Habib, Amal Robay, Mohammad Janahi, Andrea Guennoun, Evonne Chin-Smith
Purpose. Human serine/threonine kinase 4 (STK4) deficiency is a rare, autosomal recessive genetic disorder leading to combined immunodeficiency. The extent to which STK4 deficiency impairs immune signaling and host defenses is unclear. We assessed th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3596dea6dcb1d51c1d407e757dcb1daf
https://doi.org/10.21203/rs.3.rs-328827/v1
https://doi.org/10.21203/rs.3.rs-328827/v1
Autor:
Amal Al-Naimi, Indra Narang
Publikováno v:
Preterm Birth-Mother and Child
1.1 Lung development To understand the pathophysiology and the outcome of chronic lung disease of infancy, it is essential to understand normal lung development and the host of cofactors that will interfere with both antenatal and postnatal lung deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2284da9d139dd05c850ba8522f7be3
http://www.intechopen.com/articles/show/title/preterm-birth-and-long-term-pulmonary-function
http://www.intechopen.com/articles/show/title/preterm-birth-and-long-term-pulmonary-function