Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jaida Manzoor"'
Autor:
Syed Jamal Raza, Muhammad Ali, Jaida Manzoor, Waqas Imran Khan, Sabahat Amir, Mohsina Noor Ibrahim, Navira Chandio, Danish Shah Tariq, Nabeea Junaid
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 74, Iss 4 (2024)
STRUCTURED ABSTRACT Objective: The aim of this study was to measure the association between parental history of diabetes and the odds of an offspring having T1DM. Study Design: SHINE (NCT03312478) was a national, multi-center, case-control stud
Externí odkaz:
https://doaj.org/article/76a57117a74140c4bb49af2ff4da0fc5
Autor:
Sana Rafaqat, Jaida Manzoor, Rimsha Akhter, Zain Ishaque, Asifa Kamal, Faiza Saleem, Rasheeda Bashir
Publikováno v:
Journal of King Saud University: Science, Vol 35, Iss 10, Pp 102967- (2023)
Objective: Type 1 diabetes, a multigenic autoimmune disorder, is caused by the destruction of pancreatic beta-cells leads to insufficient insulin production and hyperglycemia, resulting in early morbidities and mortality. This study was designed to e
Externí odkaz:
https://doaj.org/article/447e8487538a491b9640766fb7dbb081
Autor:
Julia von Schnurbein, Jaida Manzoor, Stephanie Brandt, Friederike Denzer, Katja Kohlsdorf, Pamela Fischer-Posovszky, Mario Weißenberger, Sabine Frank-Podlech, Saqib Mahmood, Martin Wabitsch
Publikováno v:
Obesity Facts, Pp 1-16 (2019)
Background and Objective: Hyperleptinemia is supposed to play a causal role in the development of obesity-associated hypertension, possibly via increased sympathetic tone. Hence patients with congenital leptin deficiency should be hypotensive and the
Externí odkaz:
https://doaj.org/article/8faad98105fd47498d623d087454d37a
Autor:
Sommayya Aftab, Tahir Shaheen, Rameen Asif, Muhammad Nadeem Anjum, Anjum Saeed, Jaida Manzoor, Huma Arshad Cheema
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:1429-1432
Objectives Rabson Mendenhall syndrome (RMS) is a rare form of insulin resistance syndrome caused by insulin receptor mutation. In term of severity, it lies at an intermediate point on spectrum of insulin resistance with Donohue syndrome flanking the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06ef6041d78d2dfddc6af40dc5d969a5
https://doi.org/10.1515/jpem-2022-0214
https://doi.org/10.1515/jpem-2022-0214
Autor:
Julia von Schnurbein, Miriam Remy, Stephanie Brandt, Jaida Manzoor, Katja Kohlsdorf, Saqib Mahmood, Johannes Hebebrand, Martin Wabitsch
Publikováno v:
Pediatric Obesity.
Background: States of starvation are characterized by reduced physical activity and social withdrawal. This has been suggested to be mediated at least in part via reduced leptin concentrations. Objective: We therefore aimed to ascertain if leptin sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d61bccd202f756264a863256b0f396
https://doi.org/10.1111/ijpo.13057
https://doi.org/10.1111/ijpo.13057
Autor:
Sadia Saeed, Lijiao Ning, Alaa Badreddine, Muhammad Usman Mirza, Mathilde Boissel, Roohia Khanam, Jaida Manzoor, Qasim M Janjua, Waqas I. Khan, Bénédicte Toussaint, Emmanuel Vaillant, Souhila Amanzougarene, Mehdi Derhourhi, John F Trant, Anna-Maria Siegert, Brian Y. H. Lam, Giles S.H. Yeo, Layachi Chabraoui, Asmae Touzani, Abhishek Kulkarni, I. Sadaf Farooqi, Amélie Bonnefond, Muhammad Arslan, Philippe Froguel
Publikováno v:
Diabetes.
We previously demonstrated that 50% of children with obesity from consanguineous families from Pakistan carried pathogenic variants in known monogenic obesity genes. Here, we have discovered a novel monogenetic recessive form of severe childhood obes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af9660c24c88e25870fda43b98904f4a
https://doi.org/10.2337/db22-1017
https://doi.org/10.2337/db22-1017
Autor:
Philippe Froguel, Muhammad Arslan, Amélie Bonnefond, I. Sadaf Farooqi, Abhishek Kulkarni, Asmae Touzani, Layachi Chabraoui, Giles S.H. Yeo, Brian Y. H. Lam, Anna-Maria Siegert, John F Trant, Mehdi Derhourhi, Souhila Amanzougarene, Emmanuel Vaillant, Bénédicte Toussaint, Waqas I. Khan, Qasim M Janjua, Jaida Manzoor, Roohia Khanam, Mathilde Boissel, Muhammad Usman Mirza, Alaa Badreddine, Lijiao Ning, Sadia Saeed
We previously demonstrated that 50% of children with obesity from consanguineous families from Pakistan carried pathogenic variants in known monogenic obesity genes. Here, we have discovered a novel monogenetic recessive form of severe childhood obes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c723fe4a6cfa3973d43947a84428c8ef
https://doi.org/10.2337/figshare.22577353
https://doi.org/10.2337/figshare.22577353
Autor:
Sadia Saeed, Roohia Khanam, Qasim M. Janjua, Jaida Manzoor, Lijiao Ning, Sharoon Hanook, Mickaël Canouil, Muhammad Ali, Hina Ayesha, Waqas I. Khan, I. Sadaf Farooqi, Giles S.H. Yeo, Stephen O’Rahilly, Amélie Bonnefond, Taeed A. Butt, Muhammad Arslan, Philippe Froguel
BACKGROUNDBiallelic pathogenic mutations inLEP, LEPRandMC4Rgenes controlling central leptin-melanocortin signalling cause early onset severe obesity. However, the long-term clinical outcomes of leptin signalling deficiency are unknown.DESIGN AND OBJE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::342109fe0a29e661fb8df566b08ec7c0
https://doi.org/10.1101/2023.03.09.23286793
https://doi.org/10.1101/2023.03.09.23286793
Autor:
Emmanuel Vaillant, Taeed A. Butt, Philippe Froguel, Sadia M. Din, Mehdi Derhourhi, Emmanuelle Durand, Hina Ayesha, Souhila Amanzougarene, Laraib Inam, Qasim M. Janjua, Muhammad Arslan, Qura-tul Ain, Stéphane Lobbens, Alaa Badreddine, Stefan Gaget, Jaida Manzoor, Amélie Bonnefond, Waqas I. Khan, Sadia Saeed, Lionel Berberian
Publikováno v:
Diabetes. 69:1424-1438
Monogenic forms of obesity have been identified in ≤10% of severely obese European patients. However, the overall spectrum of deleterious variants (point mutations and structural variants) responsible for childhood severe obesity remains elusive. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f268c1be90afddd68606594b9e08543f
https://doi.org/10.2337/db19-1238
https://doi.org/10.2337/db19-1238
Publikováno v:
Pakistan journal of medical sciences. 38(4Part-II)
Objectives: To determine the clinical spectrum and underlying etiologies of children presented with precocious puberty at The Children’s Hospital &The Institute of Child health, Lahore. Methods: It is a retrospective review of all the children pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ae4221ada128a7917b03fa3ff665e32
https://pubmed.ncbi.nlm.nih.gov/35634621
https://pubmed.ncbi.nlm.nih.gov/35634621