Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Shahin Koohmanaee"'
Autor:
Setila Dalili, Seyyedeh Azade Hoseini Nouri, Reza Bayat, Shahin Koohmanaee, Manijeh Tabrizi, Marjaneh Zarkesh, Alireza Tarang, Nejat Mahdieh
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-6 (2023)
Abstract Background Mutations in NF1 gene could cause allelic disorders with clinical spectrum of Neurofibromatosis type 1 to Noonan syndrome. Here, a 7-year-old Iranian girl is described with Neurofibromatosis-Noonan syndrome due to a pathogenic var
Externí odkaz:
https://doaj.org/article/cc075eee30654e3784c217ff1b0fbc4b
Publikováno v:
International Archives of Otorhinolaryngology, Vol 27, Iss 03, Pp e393-e399 (2023)
Introduction Metabolic syndrome (MetS) and its associated components were reported as a possible cause of inner ear dysfunction. However, research about the influence of cardiovascular risk factors on hearing thresholds are conducted mainly in adult
Externí odkaz:
https://doaj.org/article/deb8feca1f374e25b316856df60fd556
Autor:
Setila Dalili, Reza Bayat, Seyyedeh Azade Hoseini Nouri, Shahin Koohmanaee, Manijeh Tabrizi, Marjaneh Zarkesh, Alireza Tarang
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100268- (2023)
Externí odkaz:
https://doaj.org/article/bb61dfd878804fdfa4ffd9e85b8b5260
Autor:
Shahin Koohmanaee, Seyyedeh Azadeh Hoseini Nouri, Vahid Aminzadeh, Manijeh Tabrizi, Reza Bayat, Fatemeh Kharaee, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Saber Najafi Chakoosari, Setila Dalili, Ehsan Kazemnejad Leili
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 9, Iss 1 (2023)
Background: Neuronal ceroid lipofuscinoses (NCL) is a rare progressive neurodegenerative disorder caused by more than 530 mutations of at least 13 different genes (CLN 1-14). NCL is a part of the lysosomal disease characterized by the presence of
Externí odkaz:
https://doaj.org/article/cfd2a7a53c8f4319be8462368a1ee2f9
Autor:
shahin koohmanaee, nejat mahdie, Reza Bayat, fatemeh kharaee, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Saber Najafi Chakoosari, setila dalili
Publikováno v:
Acta Medica Iranica, Pp 625-628 (2021)
Pyruvate carboxylase deficiency (PCD) is a rare autosomal recessive defect in a biotin-containing enzyme, Pyruvate carboxylase, which is considered as an enzyme of TCA-cycle regulation, gluconeogenesis, lipogenesis, and biosynthesis of neurotransmitt
Externí odkaz:
https://doaj.org/article/3f37d69eae9943418301184ba3607a54
Autor:
Shahin Koohmanaee, Amirhossein Tamimi, Soroush Ahmadimacciani, Atena Tamimi, Vahid Aminzadeh, Marjaneh Zarkesh, Seyyedeh Azadeh Hoseini Nouri, Fatemeh Rajaeipoor, Manijeh Tabrizi, Setila Dalili
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 7, Iss 4, Pp 236-243 (2021)
Background: Gonadal dysgenesis, the most common cause of primary amenorrhea, is characterized by absent or underdeveloped ovaries. Although the coexistence of gonadal dysgenesis and Mayer-Rokitansky-Küster-Hauser (MRKH) has been reported, it is stil
Externí odkaz:
https://doaj.org/article/19c98e37393143cd851b981b389bcd95
Autor:
Shahin Koohmanaee, Fatemeh Kharaee, Reza Bayat, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Saber Najafi Chakoosari, Setila Dalili, Mahsa Karambin
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 7, Iss 3, Pp 180-183 (2021)
Background: Different alleles of Fragile X Mental Retardation1 (FMR1) gene with separate molecular etiologies cause Fragile X Syndrome (FXS) and Fragile X-associated Tremor and Ataxia Syndrome (FXTAS). Premutation alleles with 55 to 200 repeats in th
Externí odkaz:
https://doaj.org/article/837b1ecb95eb4125a09b72adabf09faa
Autor:
Setila Dalili, Shahin Koohmanaee, Seyyedeh Golnaz Mirmonsef, Seyyed Amir Reza Nemati, Behrang Motamed, Manijeh Tabrizi, Mohammad Aghaeizadeh Zoroufi, Afagh Hassanzadeh Rad
Publikováno v:
International Journal of Preventive Medicine, Vol 14, Iss 1, Pp 19-19 (2023)
Background: Childhood type 1 diabetes mellitus (T1DM) is an autoimmune disease which is increasing in incidence, but little is known about the events that trigger the autoimmune process. Most of the time, these processes begin in prenatal and natal p
Externí odkaz:
https://doaj.org/article/2211203cb8c043ef8fc76dead2b74f07
Autor:
Shahin Koohmanaee, Hamidreza Badeli, Afagh Hassanzadeh Rad, Mohammad Hassan Novin, Neda Mostofizadeh, Setila Dalili, Ehsan Kazemnejad-Leili
Publikováno v:
Journal of Research in Medical Sciences, Vol 28, Iss 1, Pp 2-2 (2023)
Background: The increased prevalence of obesity in early childhood is a public health problem. Childhood obesity may affect cardiorespiratory fitness and can induce obesity and its comorbidities in adulthood. We aimed to assess childhood overweight s
Externí odkaz:
https://doaj.org/article/4bb282f8922f4d12814695f301f3ebcc
Autor:
Shahin Koohmanaee, Afagh Hassanzadeh Rad, Seyyedeh Forough Jafari, Marjaneh Zarkesh, Ehsan Kazemnejad Leili, Esfandiar Nazari, Setila Dalili
Publikováno v:
Acta Medica Iranica, Pp 127-133 (2019)
We aimed to define Metabolic Syndrome (METs) from different viewpoints to determine the most appropriate method that could be used for early METs' diagnosis in general population and treat them immediately. This study was an analytic cross-sectional
Externí odkaz:
https://doaj.org/article/f31a70aacf204485979f6f51f70e84bb