Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mozhgan Sabbaghian"'
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
Autor:
Hossein Alimadadi, Mozhgan Sabbaghian, Mehrzad Mehdizadeh, Mohammad-Hassan Moradinejad, Reihaneh Mohsenipour, Houman Alizadeh, Vahid Ziaee, Mojtaba Ranjbar
Publikováno v:
Iranian Journal of Pediatrics. 27
Background: Gastrointestinal (GI) manifestations are common in patients with Henoch Schonlein Purpura (HSP) and it seems that ultrasound is the first modality for detecting GI involvement. This study was performed to evaluate the relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eb54c12966ceb7fbd194282d2844f1e
https://doi.org/10.5812/ijp.6495
https://doi.org/10.5812/ijp.6495
Publikováno v:
Journal of Pediatric Infectious Diseases. :207-209
Neonates and young infants with human herpes virus 6 (HHV-6) may present with hepatitis, which is rarely fulminant. However, because HHV-6 is prevalent as a latent infection in humans, causality must be proven in patients with fulminant hepatitis. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::624760fa23d1bd79854e8c7b41ec23de
https://doi.org/10.3233/jpi-2010-0240
https://doi.org/10.3233/jpi-2010-0240
Publikováno v:
Gut and Liver
Background/Aims Gastroesophageal reflux disease (GERD) is common in children. Recurrent exposure to gastric acid in GERD may contribute to tooth erosion. Methods In this prospective study, 54 GERD patients qualified according to endoscopy, pH-metry,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccd418d38502e8eb3928c449537d618e
https://doi.org/10.5009/gnl.2013.7.3.278
https://doi.org/10.5009/gnl.2013.7.3.278
Autor:
Pedram, Ataee, Mehri, Najafi, Mohammad, Gharagozlou, Majid, Aflatounian, Maryam, Mahmoudi, Ahmad, Khodadad, Fatemeh, Farahmand, Farzaneh, Motamed, Glolam Hossein, Fallahi, Najmoddin, Kalantari, Habib, Soheili, Vajiheh, Modarresi, Mozhgan Sabbaghian, Modarresi, Nima, Rezaei
Publikováno v:
The Turkish journal of pediatrics. 56(2)
Zinc deficiency, which is common in patients with cystic fibrosis (CF), can lead to several complications that may increase the number of hospital admissions in this group of patients. As supplementary zinc can prevent such complications, this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0996b90853b9e5ded05f2dcca4815d35
https://pubmed.ncbi.nlm.nih.gov/24911844
https://pubmed.ncbi.nlm.nih.gov/24911844
Publikováno v:
The Turkish journal of pediatrics. 54(6)
Ulcerative colitis (UC) is a form of inflammatory bowel disease, which occasionally can be associated with autoimmune disorders. Herein, a two-year-old male infant with UC under sulfasalazine therapy is presented, who consequently developed type I di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::21da85fc3f67570f4d85706bbeb678a7
https://pubmed.ncbi.nlm.nih.gov/23692793
https://pubmed.ncbi.nlm.nih.gov/23692793
Autor:
Maurizio Averna, Angelo B. Cefalù, Mozhgan Sabbaghian, Nima Rezaei, Fatemeh Mahjoob, Mehri Najafi Sani
Publikováno v:
Scopus-Elsevier
Annals of Hepatology, Vol 10, Iss 2, Pp 221-226 (2011)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::d24d0dc32d6a3e9ef7100ea52539569a
http://hdl.handle.net/10447/79243
http://hdl.handle.net/10447/79243
Publikováno v:
European journal of pediatrics. 170(2)
Johanson-Blizzard syndrome is a very rare autosomal recessive disorder caused by mutations in the Ubiquitin-Protein Ligase E3 Component N-Recognin 1 (UBR1) gene. The syndrome is characterized by exocrine pancreatic insufficiency and a wide range of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ece7714486a8f98822d7967019da65bf
https://pubmed.ncbi.nlm.nih.gov/20556422
https://pubmed.ncbi.nlm.nih.gov/20556422
Autor:
Martin Zenker, Nima Rezaei, Mozhgan Sabbaghian, Gholam Hossein Fallahi, Manijeh Khalili, Nima Parvaneh
Publikováno v:
European journal of pediatrics. 170(2)
Johanson–Blizzard syndrome is a rare autosomal recessive disorder, characterized by exocrine pancreatic deficiency and a wide range of other abnormalities. We present here an infant with failure to thrive, exocrine pancreatic deficiency, short stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22b0c976596e7eb1b9f29ecf55b4efbb
https://pubmed.ncbi.nlm.nih.gov/20556423
https://pubmed.ncbi.nlm.nih.gov/20556423
Autor:
Farahmand, Fatemeh1, Sabbaghian, Mozhgan1 mozhgan_sabbaghian@yahoo.com, Ghodousi, Sharareh2, Seddighoraee, Nasila2, Abbasi, Mahdi3
Publikováno v:
Gut & Liver. May2013, Vol. 7 Issue 3, p278-281. 4p.