Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Parveneh Karimzadeh"'
Autor:
Yalda Nilipour, Parveneh Karimzadeh, Shahriar Nafissi, Mohammad Mahdi Taghdiri, Hedyeh Saneifard, Marjan Shakiba, Yalda Rahbarfar
Publikováno v:
International Clinical Neuroscience Journal, Vol 8, Iss 1, Pp 26-29 (2020)
Background: Lipid storage myopathies (LSMs) are rare diseases. The phenotype and genotype of lipid metabolism disorders are heterogeneous and divided into two major groups. Constant or progressive proximal and axial muscle weakness associated with or
Externí odkaz:
https://doaj.org/article/79fd93d0bafb4de7875b8c20b6637429
Autor:
Parveneh, Karimzadeh, Farzad, Ahmadabadi, Narjes, Jafari, Fakhreddin, Shariatmadari, Hamid, Nemati, Adel, Ahadi, Sanaz, Karimi Dardashti, Mehrdad, Mirzarahimi, Zahra, Dastborhan, Javad, Zare Noghabi
Publikováno v:
Iranian Journal of Child Neurology
Objective Phenylketonuria is one of the most common metabolic disorders and the first known cause of mental retardation in pediatrics. As Screening for phenylketonuria (PKU) is not a routine neurometabolic screening test for neonates in Iran, many PK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0fa541ecabc8cd66c6955379ca5dcbb3
https://pubmed.ncbi.nlm.nih.gov/24949052
https://pubmed.ncbi.nlm.nih.gov/24949052