Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Mehri Najafi Sani"'
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2017 (2017)
Background. Eosinophilic esophagitis is an inflammatory condition where there is a dense infiltration of eosinophils typically exceeding fifteen cells per high power field. Familial Mediterranean fever is an autosomal recessive disorder characterized
Externí odkaz:
https://doaj.org/article/96e60ac131b64a849905898d45bb8bcd
Autor:
Mehri Najafi Sani, Mozhgan Sabbaghian, Fatemeh Mahjoob, Angelo B. Cefalù, Maurizio R. Averna, Nima Rezaei
Publikováno v:
Annals of Hepatology, Vol 10, Iss 2, Pp 221-226 (2011)
Abetalipoproteinemia (ABL), or Bassen-Kornzweig syndrome, is a rare autosomal recessive disorder of lipoprotein metabolism, characterized by fat malabsorption, hypocholesterolemia retinitis pigmentosa, progressive neuropathy and acanthocytosis from e
Externí odkaz:
https://doaj.org/article/b69ac4a00b324f64b203dbf54dab8a6e
Publikováno v:
Acta Medica Iranica, Vol 53, Iss 10 (2015)
Zellweger syndrome (ZS) is a peroxisomal disorder with a multiple congenital anomalies, characterized by stereotypical facies, profound hypotonia, organ involvement including cerebral, retinal, hepatic, and renal. Herein, a 3-month-old female with ZS
Externí odkaz:
https://doaj.org/article/1967fa6f340946f08b48300147dac55b
Autor:
Fatemeh Mahjoub, Mehri Najafi Sani, Ahmad Khaleghnejad Tabari, Maryam Monajemzadeh, Saeed Zandieh
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 02, Iss 01, Pp 029-031 (2013)
Abstract Introduction Protein losing enteropathy is a symptom characterized by loss of protein in intestines resulting in low protein levels in serum and generalized edema. Several causes are reported for this condition. Hereby we report an as yet
Externí odkaz:
https://doaj.org/article/0441294a8eb848ec9ac5e7299debc62f
Publikováno v:
International Journal of Fertility and Sterility, Vol 4, Iss 2, Pp 85-87 (2010)
Cystic fibrosis (CF), the most common life-shortening, hereditary disease in whites, manifests itself principally in childhood. Patients presenting with CF as adults appear to be different when compared to patients diagnosed with CF during childhood.
Externí odkaz:
https://doaj.org/article/92f356594afd418185eb5fc8d832a072
Autor:
Kambiz Eftekhari, Farzaneh Motamed, Hamid Reza Sadeghi, Mehri Najafi Sani, Fatemeh Farahmand, Gholam Hosein Fallahi, Hosein Alimadadi
Publikováno v:
Journal of Comprehensive Pediatrics. 11
Background: Benign esophageal strictures are not rare. Over the past two decades, endoscopic balloon dilatation (EBD) has been used to treat them. Objectives: The purpose of this study was to identify the most common causes of benign esophageal stric
Autor:
Farzaneh Motamed, Gholamhosein Fallahi, Seyed Mohammad Mir Eskandari, Pejman Rohani, Fatemeh Farahmand, Aliraza Moravveji, Hosein Alimadadi, Mehri Najafi-Sani
Publikováno v:
Iranian Journal of Pediatrics. 28
Background: Effective and safe procedural sedation is necessary for percutaneous liver biopsy in children. There are a number of different protocols for this purpose. The current study investigated ketamine and DPT cocktail (meperidine (Demerol®) +
Autor:
Ebrahim Ghaderi, Pedram Ataee, Vahidreza Afrasiabi, Bahram Nikkhoo, Mehri Najafi Sani, Froozan Kariminejhad, Asadollah Fathollahpour, Jaleh Parizad, Banafsheh Sedaghat, Ramesh Rahehagh, Kambiz Eftekhari, Maryam Monajemzadeh
Publikováno v:
Iranian Journal of Pediatrics. 27
Background: Chronic abdominal pain in children is a common disorder. For an accurate diagnosis of its cause, sometimes invasive diagnostic procedures such as endoscopy should be performed. Objectives: The purpose of the study was to evaluate the feca
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2017 (2017)
Case Reports in Gastrointestinal Medicine
Case Reports in Gastrointestinal Medicine
Background. Eosinophilic esophagitis is an inflammatory condition where there is a dense infiltration of eosinophils typically exceeding fifteen cells per high power field. Familial Mediterranean fever is an autosomal recessive disorder characterized
Autor:
Mehri Najafi Sani, Fatemehsoltan Zegheibizadeh, Seyed Ali Jafari, Monnavar Afzal Aghaee, Hamid Ahanchian, Hamid Reza Kianifar
Publikováno v:
International Journal of Pediatrics, Vol 1, Iss 1, Pp 19-24 (2013)
Introduction To define the clinical features, biochemical and histological findings and outcome of three forms of autoimmune hepatitis. Materials and Methods In a cross sectional study between November 2001 to January 2008 in Tehran and Mashhad unive