Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Arya Sotoudeh"'
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:
Acta Medica Iranica, Vol 55, Iss 10 (2017)
Pericentric inversion of Chromosome 9 is one of the most common chromosomal abnormalities, which could be associated with various manifestations in some cases. Herein, a patient is presented with ambiguous genitalia that karyotyping revealed pericent
Externí odkaz:
https://doaj.org/article/9ccb883efa404322bebcfc867c2f9de4
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
Autor:
Parastoo Rostami, Farzaneh Abbasi, Arya Sotoudeh, Azadeh Sayarifard, Mehrzad Mehdizadeh, Fatemeh Sayarifard, Ali Rabbani, Leyla Katebi
Publikováno v:
Mediterranean Journal of Rheumatology. 34:44
Autor:
Babak, Aghili, Ali Akbar, Amirzargar, Asadollah, Rajab, Ali, Rabbani, Arya, Sotoudeh, Sara, Assadiasl, Bagher, Larijani, Ahmad, Massoud
Publikováno v:
Iranian journal of immunology : IJI. 12(4)
Type 1 diabetes (T1D) is a T cell mediated autoimmune disease targeting the insulin-producing β cells within pancreatic islets. Autoimmune diseases may develop as a consequence of altered balance between regulatory (Tregs) and autoreactive T cells.T
Autor:
Faezeh-Moghimpour Bijani, Ali Rabbani, Maryam Nakhaeimoghadam, Nima Rezaei, Arya Sotoudeh, Pascale Hilbert, Parastoo Rostami
Publikováno v:
Annales d'Endocrinologie. 74:59-61
Berardinelli-Seip congenital lipodystrophy (BSCL) syndrome is an autosomal recessive disorder, caused by mutation in the AGPAT2 gene, which could lead to insulin resistance and variety of complications. Herein, a 7-year old girl is presented with gen
Publikováno v:
The Turkish journal of pediatrics. 54(3)
Despite the essential role of insulin in the management of patients with diabetes mellitus type 1, insulin use can cause a variety of adverse effects, such as hypoglycemia and weight gain. Herein, we describe an adolescent girl with type 1 diabetes m
Autor:
Mojgan Karbakhsh, Kazem Mohammad, Ali Rabbani, Nima Parvaneh, Karamatallah Nouri, Ali Salavati, Shahnaz Khodai, Arya Sotoudeh
Publikováno v:
Scopus-Elsevier
Background: Entering puberty is an important milestone of human growth and maturation associated with marked physiological and psychological changes. Aim: To assess normal pubertal development in Iranian girls to define normal and precocious puberty.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a949bacabe3677430669f761cf74da16
http://www.scopus.com/inward/record.url?eid=2-s2.0-51349087162&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-51349087162&partnerID=MN8TOARS