Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hussein Al Kindi"'
Autor:
Sumaya Al Oraimi, Khoula Al Shidhani, Hasina Al Harthi, Suaad Al Sinani, Nasser Al Busaidi, Muna Al Bimani, Qasem Al Salmi, Hussein Al Kindi
Publikováno v:
Oman Medical Journal, Vol 37, Iss 6, Pp e444-e444 (2022)
Objectives: To describe the demographic distribution of cystic fibrosis (CF) in Omani children, estimate the national prevalence, and provide updated mutational panels of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Methods: W
Externí odkaz:
https://doaj.org/article/caf6c221582e4acd8551f55e58864cad
Publikováno v:
Oman Medical Journal, Vol 36, Iss 6, Pp e319-e319 (2021)
Superior herniation of normal mediastinal thymus is a rare cause of anterior neck swelling, and only a few cases are reported in the literature. It clinically presents as a suprasternal swelling in the neck that appears during increased intrathoracic
Externí odkaz:
https://doaj.org/article/69ba187c6f9c44c797ead8f4c06c0e72
Autor:
Issa K. Al-Nuumani, Abdulaziz Bakathir, Ahmed Al-Hashmi, Mohammed Al-Abri, Hussein Al-Kindi, Intisar Al-Macki, Zainab Al-Balushi
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 18, Iss 3, Pp 379-382 (2018)
The surgical management of paediatric patients with temporomandibular joint (TMJ) ankylosis, mandibular retrognathia and obstructive sleep apnoea (OSA) is challenging. We report a nine-year-old boy who presented to the Department of Oral Health, Sult
Externí odkaz:
https://doaj.org/article/3cfa3bb880994beb84755f9cbf2844bb
Autor:
Hussein Al-Kindi, Al-Shaima Al-Abri, Tabinda Naz, Doaa Khater, Saif Al-Yaarubi, Mohamed Al-Abri
Publikováno v:
Sleep and Breathing. 26:815-821
Sanjad Sakati syndrome (SSS) is a rare autosomal recessive genetic disorder caused by mutation in TBCE (tubulin folding cofactor E) gene. Reported cases were almost exclusively of Middle-Eastern and Arabian children of consanguineous parents. We repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da6bbd2ea58147e9ab22f8aa166e694
https://doi.org/10.1007/s11325-021-02463-4
https://doi.org/10.1007/s11325-021-02463-4
Autor:
Salem Al-Tamemi, Hussein Al-Kindi
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 9, Iss 2, Pp 170-174 (2009)
Pulmonary haemorrhage is usually secondary to a systemic disease affecting the lung with or without other organ involvement. Idiopathic pulmonary haemorrhage is a diagnosis of exclusion; as described in the literature, it is a rare disease. We report
Externí odkaz:
https://doaj.org/article/0ea8cc3137954602b297d63117fdc9dc
Autor:
Saif, Al-Yaarubi, Al-Shaima, Al-Abri, Hussein, Al-Kindi, Mohamed, Al-Abri, Tabinda, Naz, Doaa, Khater
Publikováno v:
Sleepbreathing = SchlafAtmung. 26(2)
Sanjad Sakati syndrome (SSS) is a rare autosomal recessive genetic disorder caused by mutation in TBCE (tubulin folding cofactor E) gene. Reported cases were almost exclusively of Middle-Eastern and Arabian children of consanguineous parents. We repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::475e5dee2b4a84e58f19824f278c2cea
https://pubmed.ncbi.nlm.nih.gov/34368942
https://pubmed.ncbi.nlm.nih.gov/34368942
Autor:
Abdulhakim Al Rawas, Hussein Al Kindi, Tabinda Naz Qureshi, Syed Rizwan Haider, Khalfan S. Al Senaidi, Rashid Al Sukaiti, Mohamed Ebrahim Mohamed Ebrahim Elshinawy, Yasser Wali
Publikováno v:
Journal of pediatric hematology/oncology. 42(6)
Pulmonary artery aneurysms and pseudoaneurysms are rare vascular anomalies in children that can lead to massive hemoptysis resulting in severe morbidity and even mortality. High level of clinical suspicion, timely diagnosis, and prompt management are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60a8470ecde0d1eb542c99e7089fd1ff
https://pubmed.ncbi.nlm.nih.gov/31449497
https://pubmed.ncbi.nlm.nih.gov/31449497
Autor:
Hussein Al-Kindi, A. Bakathir, Issa K Al-Nuumani, Mohammed Al-Abri, Zainab Al-Balushi, Ahmed Al-Hashmi, Intisar Al-Macki
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 18, Iss 3, Pp 379-382 (2018)
The surgical management of paediatric patients with temporomandibular joint (TMJ) ankylosis, mandibular retrognathia and obstructive sleep apnoea (OSA) is challenging. We report a nine-year-old boy who presented to the Department of Oral Health, Sult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cce9cd467908da1abc7bc1690166ae1f
https://doi.org/10.18295/squmj.2018.18.03.019
https://doi.org/10.18295/squmj.2018.18.03.019
Autor:
Zainab Al-Balushi, A.M. Varghese, A. Bakathir, S. Al-Azri, A. Al-Hashmi, S.R. Haider, I. Macki, Hussein Al-Kindi
Publikováno v:
International Journal of Oral and Maxillofacial Surgery. 46:356
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473c9f849b8c79bcf5f1b79f756097c4
https://doi.org/10.1016/j.ijom.2017.02.1200
https://doi.org/10.1016/j.ijom.2017.02.1200
Autor:
Salem Al-Tamemi, Hussein Al-Kindi
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 9, Iss 2, Pp 170-174 (2009)
Pulmonary haemorrhage is usually secondary to a systemic disease affecting the lung with or without other organ involvement. Idiopathic pulmonary haemorrhage is a diagnosis of exclusion; as described in the literature, it is a rare disease. We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d1fc37020d4e3db5cab43d0a54d9d903
https://pubmed.ncbi.nlm.nih.gov/21509296
https://pubmed.ncbi.nlm.nih.gov/21509296