Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Manijeh Tabrizi"'
Autor:
Manijeh Tabrizi, Seyyedeh Azade Hoseini Nouri, Afagh Hasanzade Rad, Setila Dalili, Seyede Tahoura Hakemzadeh, Amir Mohammad Ghanbari, Reza Bayat, Amir Reza Mashaei, Nazanin Medghalchi, Kamyar Khosravi
Publikováno v:
Journal of Pediatrics Review, Vol 11, Iss 2, Pp 163-170 (2023)
Background: Bedside teaching is a concentrated form of small-group teaching that takes place in the presence of the patient. Improvement in communication skills in a sympathetic manner with the patient and the ability to provide a purposeful history
Externí odkaz:
https://doaj.org/article/31cbacc37e8e409f96e186d7ae6925d4
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
Autor:
Seyyedeh Azade Hoseini Nouri, Manijeh Tabrizi, Marjaneh Zarkesh, Ali Talebi, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Setila Dalili, Ehsan Kazemnezhad Leili
Publikováno v:
Journal of Pediatrics Review, Vol 10, Iss 4, Pp 287-296 (2022)
Background and Objectives: Over the past three decades, the prevalence of overweight and obesity in children and adolescents has increased up to 3 times. Obesity is a multi-systemic medical problem affecting all socioeconomic statuses and increases t
Externí odkaz:
https://doaj.org/article/73c4b9caeada4e38958faea36f19d3d6
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:
Marjaneh Zarkesh, Sadroddin Mahdipour, Safoora Aghili, Atefeh Jafari, Seyyedeh Azadeh Hoseini Nouri, Afagh Hassanzadeh Rad, Maryam Ghalandari, Manijeh Tabrizi
Publikováno v:
PLoS ONE, Vol 18, Iss 12 (2023)
Externí odkaz:
https://doaj.org/article/94857fe7dd044d0eabb07887d54cc1eb
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, 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 Koomanaee, Setila Dalili, Seyyedeh Azade Hoseini Nouri, Seyedeh Zohreh Jalali, Manijeh Tabrizi, Ghazaleh Aldaghi, Afagh Hassanzadeh Rad
Publikováno v:
Acta Medica Iranica, Vol 60, Iss 9 (2022)
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder with homozygous or heterozygous mutations in one of the five following genes (ORC1, ORC4, ORC6, CDT1, and CDC6). This syndrome is characterized by the triad of short stature (pre/post
Externí odkaz:
https://doaj.org/article/c19c7dd67ee945e3b31aea0b7d348cca
Autor:
Manijeh Tabrizi, Sima Sarabi, Morteza Rahbar Taramsari, Adel Baghersalimi, Afagh Hassanzadeh Rad, Bahram Darbandi
Publikováno v:
Iranian Journal of Toxicology, Vol 15, Iss 3, Pp 151-156 (2021)
Background: Poisoning comprises about 7% of accidents in children under 5-year-old and 2% of all pediatric deaths in developing countries. To warn against and prevent future potential poisoning with opioid substances, this comparative study was condu
Externí odkaz:
https://doaj.org/article/cadfe7cf4ec743199b5fe91e0e58f78e
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