Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Shahab, Noorian"'
Autor:
Shahab Noorian, Sepideh Hamzehlou, Ali Rabbani, Arya Sotoudeh, Kioumars Pour Rostami, Shahram Savad
Publikováno v:
Basic and Clinical Neuroscience, Vol 12, Iss 4, Pp 563-568 (2021)
Introduction: Allan-Herndon-Dudley Syndrome (AHDS) is a rare X-linked recessive intellectual disability condition with neuromuscular involvements. Altered thyroid function tests are major milestones in AHDS diagnosis. However, due to phenotypic varia
Externí odkaz:
https://doaj.org/article/fb63f76045ee4c94861c790665d6b0e4
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 3, Pp 216-219 (2021)
Objective: Kallmann syndrome (KS) may be accompanied by anosmia or hyposmia and midline defects. We present an overweight 16-year-old boy with a lack of puberty, anosmia, congenital right eye ptosis, and normal intellectual function. Methods: Testicu
Externí odkaz:
https://doaj.org/article/97f1fc819e994e4c8d74e98e0c5560f1
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2020)
Multiple sulfatase deficiency (MSD) is a lysosomal storage disorder (LSD) that results in the accumulation of sulfate esters which go on to cause neurological deterioration and mental delay, skin changes, and dysmorphism. The disease can be categoriz
Externí odkaz:
https://doaj.org/article/fce61c8df0584e66bfec797b76004cb5
Publikováno v:
Journal of Diabetes & Metabolic Disorders. 21:1591-1597
Type 1 diabetes mellitus (T1DM) is a chronic metabolic disorder, and its prevalence and incidence are increasing globally. Insulin therapy is the basis of T1DM management that can prevent numerous complications. Identifying and resolving the factors
Autor:
Shahram Savad, Kioumars Pour Rostami, Arya Sotoudeh, Ali Rabbani, Shahab Noorian, Sepideh Hamzehlou
Publikováno v:
Basic and Clinical Neuroscience, Vol 12, Iss 4, Pp 563-568 (2021)
Introduction: Allan-Herndon-Dudley Syndrome (AHDS) is a rare X-linked recessive intellectual disability condition with neuromuscular involvements. Altered thyroid function tests are major milestones in AHDS diagnosis. However, due to phenotypic varia
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 3, Pp 216-219 (2021)
AACE Clinical Case Reports
AACE Clinical Case Reports
Objective Kallmann syndrome (KS) may be accompanied by anosmia or hyposmia and midline defects. We present an overweight 16-year-old boy with a lack of puberty, anosmia, congenital right eye ptosis, and normal intellectual function. Methods Testicula
Publikováno v:
Twin research and human genetics : the official journal of the International Society for Twin Studies. 25(2)
Mitochondrion regulates cellular metabolism with the aid of its respiratory complexes; any defect within these complexes can result in mitochondrial malfunction and various conditions. One such mutation can occur in SLC25A10, resulting in mitochondri
Autor:
Mehrnaz Mesdaghi, Mazdak Fallahi, Samaneh Parviz, Zahra Chavoshzadeh, Fatemeh Aghamahdi, Mahnaz Jamee, Mehdi Moosavian, Elahe Dolatshahi, Mohammad Reza Alaei, Gholamreza Azizi, Shahab Noorian, Habibeh Taghavi Kojidi
Publikováno v:
Immunological Investigations. 51:778-786
Autoimmune disorders are reported as presenting signs in patients with immunoglobulin A (IgA) deficiency. Herein, we aim to evaluate serum IgA among patients with autoimmune polyendocrinopathy.Patients with two or more autoimmune endocrinopathies wer
Publikováno v:
J Diabetes Metab Disord
Familial Hypercholesterolemia is an autosomal, dominant genetic disorder associated with premature cardiovascular disease (CVD). Mutations in the LDLR, APOB, and PCSK9 genes cause the FH phenotype, but in 20% of FH patients, mutations in other genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cbbf34e41ebb6bd2c7f4e208d0e0506
https://europepmc.org/articles/PMC9167334/
https://europepmc.org/articles/PMC9167334/
Publikováno v:
International Journal of Enteric Pathogens. 9:78-80
Since the World Health Organization (WHO) announced the severe acute respiratory syndrome coronavirus 2 pandemic, different cases with various diseases have been reported along with the coronavirus disease 2019 (COVID-19). Although COVID-19 is less c