Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Davoud Amirkashani"'
Autor:
Davoud Amirkashani, Saeid Talebi, Mohammad Vafaei shahi, Ali Zekri, Parisa Abdi, Mahdokht Mehramiz
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102044- (2024)
Purpose: To report a 15 year old girl with citrullinemia type 1 and 2 accompanied by neurologic signs and symptoms and a novel ocular complaint in cornea like tyrosinemia type 2. Observations: A 15 year old female was admitted with decreased consciou
Externí odkaz:
https://doaj.org/article/b67369ce6fd34627a382705ecba54594
Autor:
Davoud Amirkashani, Farzaneh Rohani, Mahmoud Khodadost, Rozita Hoseini, Hamidreza Alidoost, Sedigheh Madani
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Introduction We investigated the age of starting Estrogen replacement therapy as a key parameter for reaching near normal Final Height (FH) in Chronic Kidney Disease (CKD) girls with growth retardation. Method This open label, quasi-experime
Externí odkaz:
https://doaj.org/article/ff7b7061579c4b09920dd71ed592e9f8
Autor:
Fahimeh Soheilipour, Mohammad Ebrahimian, Mohadeseh Pishgahroudsari, Maryam Hajian, Davoud Amirkashani, Mahtab Ordooei, Mohammad Radgoodarzi, Delaram Eskandari
Publikováno v:
BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background The prevalence of obesity is considered to be increased worldwide. Lack of mineral elements is one of the essential side effects of bariatric surgery as a trending treatment for obesity. We aimed to assess zinc deficiency among mo
Externí odkaz:
https://doaj.org/article/cad1e428317e47fdb9e71aa89f02271c
Publikováno v:
Endocrine Connections, Vol 7, Iss 3, Pp 456-459 (2018)
Background: This study was conducted to find out whether boys with constitutional delay in growth and puberty (CDGP) could attain their target height and predicted adult height (PAH) in adulthood or not. Methods: After measuring the height, weight,
Externí odkaz:
https://doaj.org/article/5850b99ab8ea4734ae1c8d0d756acfcc
Autor:
Mahtab Rouhifard, Fatemeh Bandarian, Hamid Reza Aghayan, Reihaneh Mohsenipour, Babak Arjmand, Sedighegh Madani, Sepideh Alavi-Moghadam, Davoud Amirkashani, Aria Setudeh, Parastoo Rostami, Bagher Larijani, Negar Rezaei
Publikováno v:
J Diabetes Metab Disord
INTRODUCTION: Type 1 Diabetes Mellitus (T1DM) is an auto immune reaction against insulin secreting beta cells. Exogenous insulin administration is the only standard treatment for T1DM. However, despite tight glycemic control many patients will develo
Autor:
Davoud Amirkashani, Sedigheh Madani
Publikováno v:
Journal of Diabetes & Metabolic Disorders. 22:897-898
Publikováno v:
World Journal of Peri & Neonatology.
Background: Niemann-Pick disease type C (NPC) is an autosomal recessive neurovisceral lysosomal storage disorder resulting from mutations in either the NPC1 or the NPC2 gene. It shows a broad spectrum of clinical phenotypes and a variable age at diag
Publikováno v:
Clinical neurology and neurosurgery. 215
This is a case report of Methenyl Tetrahydrofolate synthetase deficiency (MTHFS deficiency) characterized by global developmental delay, cerebral hypomyelination, severe spastic tonicity in extremities, and microcephaly. Mutation in the MTHFS gene wa
Autor:
Saeed R. Ghaffari, Maryam Rafati, Mahdi Shadnoush, Shokooh Pourbabaee, Mohammad Aghighi, Siamak Mirab Samiee, Jamshid Kermanchi, Mohammad R. Alaei, Shadab Salehpour, Davoud Amirkashani, Aria Setoodeh, Peymaneh Sarkhail, Reza Shervin Badv, Majid Aminzadeh, Siamak Shiva, Peyman Eshraghi, Hossein Moravej, Mahin Hashemipour, Noushin Rostampour, َAmir Ali Hamidieh, Bibi Shahin Shamsian, Sedigheh Shams, Daniel Zamanfar, Ayoub Ebrahimi, Ali Otadi, Seyedeh Zahra Tara, Zeinab Barati, Laya Fakhri, Azadeh Hoseini, Hosna Amiri, Somayeh Ramandi, Niusha Mostofinezhad, Zahra Pahlevani Kani, Elham Mohammadyari, Mahsa Khosravi, Masoome Saadati, Fatemeh Hoseininasab, Hamid Reza Khorram Khorshid, Younes Modaberisaber
Publikováno v:
Human mutationREFERENCES. 43(4)
Mucopolysaccharidoses (MPSs) are rare, heterogeneous inborn errors of metabolism (IEM) diagnosed through a combination of clinical, biochemical, and genetic investigations. The aim of this study was molecular characterization of the largest cohort of
Autor:
Sara Pajouhanfar, Roberto Colombo, Parvin Mansouri, Leila Youssefian, Ketty Peris, Soheila Sotoudeh, Sirous Zeinali, Hassan Vahidnezhad, Davoud Amirkashani, Michael A. Levine, Amir Hossein Saeidian, Jouni Uitto
Publikováno v:
J Hepatol
Background & Aims Non-alcoholic fatty liver disease (NAFLD) is a multifactorial condition and the most common liver disease worldwide, affecting more than one-third of the population. So far there have been no reports on mendelian inheritance in fami