Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sara G. Hamad"'
Publikováno v:
Case Reports in Immunology, Vol 2023 (2023)
Background. Drug reaction with eosinophilia and systemic symptoms (DRESSs) syndrome is an idiosyncratic drug-induced reaction that rarely occurs in children but can lead to serious complications. It manifests most commonly with fever, extensive skin
Externí odkaz:
https://doaj.org/article/5ab2b016a4b14f8daee58cbc885df33c
Publikováno v:
Respiratory Medicine Case Reports, Vol 41, Iss , Pp 101786- (2023)
Airway webs are abnormal fibrous membranes in the airway lumen that rarely occur but can lead to serious or even life-threatening symptoms because of critical airway obstruction. Airway webs can be acquired or congenital. Acquired webs are likely to
Externí odkaz:
https://doaj.org/article/a3ea47bb16764c8e84dc3c2df937561c
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:
Children, Vol 9, Iss 2, p 252 (2022)
Allergic bronchopulmonary aspergillosis (ABPA) is an immune-mediated inflammatory airway disease that predominantly affects patients with cystic fibrosis (CF) and, less commonly, patients with asthma. ABPA can lead to irreversible lung injury and bro
Externí odkaz:
https://doaj.org/article/8e7143cd6eb448b8870b2dc5c6d0e7bc
Autor:
Mohamed A Hendaus, Amna M Al-Khuzaei, Osama Samarah, Sara G Hamad, Basma A Selim, Walid El Ansari
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 9, Iss 6, Pp 3053-3059 (2020)
Purpose: To identify parental awareness and knowledge regarding child abuse and neglect in the State of Qatar. Methods: A cross-sectional study using a questionnaire was conducted at Hamad Medical Corporation, the only tertiary pediatric hospital in
Externí odkaz:
https://doaj.org/article/df5ef395718b4473aec68473401df452
Autor:
Amal AlNaimi, Sara G. Hamad, Reem B. A. Mohamed, Tawfeg Ben‐Omran, Khalid Ibrahim, Mahmoud F. El‐Said Osman, Mutasim Abu‐Hasan
Publikováno v:
Pediatric Pulmonology. 58:1004-1011
Spinal muscular atrophy (SMA) is an inherited progressive neuromuscular disorder characterized by generalized hypotonia, respiratory failure and early death. The introduction of gene replacement therapy (GRT) modified the natural history of the disea
Publikováno v:
Kompass Neumología. 4:105-110
La aspergilosis broncopulmonar alérgica (ABPA) es una enfermedad inflamatoria de las vías respiratorias, de origen inmunitario, que afecta principalmente a pacientes con fibrosis quística (FQ) y, con menor frecuencia, a pacientes con asma. La ABPA
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