Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Afagh Hassanzadeh Rad"'
Autor:
Mohammad Samami, Fereshteh Najar-Karimi, Babak Bakhshayesh Eghbali, Aghil Hosseinpour Sanati, Afagh Hassanzadeh Rad
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Introduction Headache is an illness with high prevalence and adverse effects on quality of life. As oral or dental problems such as pain can trigger or aggravate it, we aimed to investigate and compare oral and dental health status in patien
Externí odkaz:
https://doaj.org/article/22b0053f17674b1ebcd01a7f53287b3c
Autor:
Kaveh Gharaei Nejad, Abbas Darjani, Narges Alizadeh, Seyede Tahoura Hakemzadeh, Afagh Hassanzadeh Rad, Ehsan Kazemnejad-Leili, Reyhaneh Ghadarjani, Hojat Eftekhari, Rana Rafiei, Setila Dalili
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 4, Pp 659-665 (2024)
Background: Acne vulgaris is a chronic, inflammatory disease and one of the most common skin diseases. Isotretinoin is the best treatment for severe nodulocystic acne compared to other systemic medicine. Although serum lipids elevation is one of the
Externí odkaz:
https://doaj.org/article/ee546ad2e7084d429e501d92c27616a4
Autor:
Afagh Hassanzadeh Rad, Vahid Aminzadeh
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 10, Iss 2, Pp 146-149 (2024)
Background: Idiopathic intracranial hypertension (IIH) or pseudotumor cerebri is a rare disorder. Regarding the latest diagnostic criteria for this disorder, we present a rare case of IIH. Case presentation: The case was an 11-year-old girl referred
Externí odkaz:
https://doaj.org/article/bd4ca6e4812d4eb3a144c51a669caeb4
Autor:
Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi, Afagh Hassanzadeh Rad, Reza Bayat, Bahareh Rabbani, Nejat Mahdieh
Publikováno v:
International Journal of Endocrinology, Vol 2024 (2024)
Familial glucocorticoid deficiency is caused by variants in the MC2R and MRAP genes. We report an Iranian patient with congenital glucocorticoid deficiency and cholestasis due to pathogenic variants in the MC2R gene. This is the first documented case
Externí odkaz:
https://doaj.org/article/54a13b6b80f2438eb241494b03736e52
Autor:
Afagh Hassanzadeh Rad, Niloufar Nazeri
Publikováno v:
Journal of Nephropharmacology, Vol 13, Iss 1, Pp e10632-e10632 (2024)
Gestational diabetes mellitus (GDM) is a complication of pregnancy defined as any level of early or first detection of glucose intolerance in pregnancy. It is a prevalent metabolic disorder associated with several maternal and neonatal complications.
Externí odkaz:
https://doaj.org/article/9175c51a6df34103821a8b5013405dbe
Autor:
Mohammad Soleimani, Seyed Ali Tabatabaei, Arash Mirzaei, Amirreza Esfandiari, Mahdi Soleymanzadeh, Reza Sadeghi, Afagh Hassanzadeh Rad
Publikováno v:
Oman Journal of Ophthalmology, Vol 16, Iss 1, Pp 69-74 (2023)
BACKGROUND: Keratoconjunctivitis is one of the most common pathologies worldwide, caused by several infectious and noninfectious factors. This study aimed to determine the effect of povidone-iodine 2% eye drops in treating adenoviral keratoconjunctiv
Externí odkaz:
https://doaj.org/article/45dca09148034939affa1555fafedd2a
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:
Mahin Hashemipour, Daniel Zamanfar, Houman Hashemian, Afagh Hassanzadeh Rad, Maryam Shahrokhi, Setila Dalili
Publikováno v:
Journal of Pediatrics Review, Vol 10, Iss Special Issue, Pp 397-402 (2022)
Background: COVID-19 is an unknown and novel virus that creates a challenge with all comorbid conditions, including diabetes mellitus (DM). Although DM has not been determined as a definite risk factor for COVID-19 in childhood, clinicians should con
Externí odkaz:
https://doaj.org/article/6927af09642c47a69bb8407e7c08afe0
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