Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Leila Bani Adam"'
Autor:
Fereshteh Salari, Leila Bani Adam, Saba Arshi, Mohammad Hassan Bemanian, Morteza Fallahpour, Mohammad Nabavi
Publikováno v:
Journal of Pediatrics Review, Vol 7, Iss 4, Pp 223-228 (2019)
Introduction: Netherton Syndrome (NS) is a rare hereditary autosomal recessive disorder with ichthyosiform cutaneous lesions, specific hair shaft defect, and atopic diathesis. The incidence of NS is estimated to be approximately 1 in 200000. The obje
Externí odkaz:
https://doaj.org/article/4f57275d71b74b2f93acb18eb8a7ac05
Autor:
Fatemeh Nayeri, Mamak Shariat, Hosein Dalili, Leila Bani Adam, Fatemeh Zareh Mehrjerdi, Afsaneh Shakeri
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 10, Iss 2, Pp 137-140 (2012)
Background: Asphyxia is a medical condition in which placental or pulmonary gas exchange is impaired or they cease all together, typically producing a combination of progressive hypoxemia and hypercapnea. Objective: In addition to regional difference
Externí odkaz:
https://doaj.org/article/173ac91538544f7c9fe81092b94b64bb
Autor:
Saba Arshi, Fereshteh Salari, Morteza Fallahpour, Mohammad Hassan Bemanian, Leila Bani Adam, Mohammad Nabavi
Publikováno v:
Journal of Pediatrics Review, Vol 7, Iss 4, Pp 223-228 (2019)
Introduction: Netherton Syndrome (NS) is a rare hereditary autosomal recessive disorder with ichthyosiform cutaneous lesions, specific hair shaft defect, and atopic diathesis. The incidence of NS is estimated to be approximately 1 in 200000. The obje