Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Umm e-Kalsoom"'
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 98, Iss 5, Pp 580-586 (2023)
Abstract Background Ectodermal dysplasia syndactyly syndrome 1 (EDSS1) is a rare hereditary disorder characterized by defects in teeth, hair, and nails in association with a fusion of the digits. Genetically, the disease phenotypes are caused by homo
Externí odkaz:
https://doaj.org/article/9da5350d3906421fa84ae0ce4524d6bc
Autor:
Hajra, Bibi, Abdullah, Bibi, Nousheen, Syed, Fibhaa, Ullah, Asmat, Ahmad, Wasim, Umm-e-Kalsoom
Publikováno v:
In Anais Brasileiros de Dermatologia September-October 2023 98(5):580-586
Publikováno v:
Journal Riphah College of Rehabilitation Sciences, Vol 10, Iss 01 (2022)
Background: Stroke can occur due to blockage or blood vessels’ hemorrhage which supply blood to brain. Post-stroke shoulder pain (PSSP) is very common after stroke. It is present even during resting condition and affects active and passive movement
Externí odkaz:
https://doaj.org/article/755df33e838543a397ecccc7e7b78c19
Publikováno v:
Health Science Reports, Vol 5, Iss 2, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/15d45fe877394cc69ca3e70b3215a16d
Autor:
Jhanzeb Iftikhar, Fareeha Sheikh, Nazish Khalid, Syed Abdul Mannan Hamdani, Usman Ahmad, Umm-E-Kalsoom Awan
Publikováno v:
Asian Pacific Journal of Cancer Care, Vol 6, Iss 3, Pp 349-351 (2021)
Dermatofibrosarcoma protuberans (DFSP) is an uncommon, low grade, malignant fibroblastic tumor. Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by dysregulated production of granulocytic cell line without the loss of the
Externí odkaz:
https://doaj.org/article/0d0f90793b31437d943317489b543cd7
Autor:
Sher Alam Khan, Saadullah Khan, Noor Muhammad, Zia Ur Rehman, Muhammad Adnan Khan, Abdul Nasir, Umm-e- Kalsoom, Anwar Kamal Khan, Hassan Khan, Naveed Wasif
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Background: The syndromic and non-syndromic congenital missing teeth phenotype is termed tooth agenesis. Since tooth agenesis is a heterogeneous disorder hence, the patients show diverse absent teeth phenotypes. Thus identifying novel genes involved
Externí odkaz:
https://doaj.org/article/d192e4165b5d41ef8804a34ee100dbeb
Autor:
Mussadique Ali, Chandumal ., Manzoor Khan, Jhanzeb Iftikhar, Samia Yasmeen, Umm e Kalsoom Awan
Publikováno v:
Pakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 719-21 (2021)
Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infreq
Externí odkaz:
https://doaj.org/article/48eef3b98d3d45d99e9a296a81340b40
Autor:
Tayyaba Afzal, Ghazala Kaukab Raja, Maimoona Afzal, Shakeel Ahmad, Nighat Sultana, Umm e Kalsoom
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 1 (2020)
Polycystic ovary syndrome (PCOS) is an oligogenic condition, characterised by hyperandrogenism, ovulatory dysfunction and polycystic ovarian morphology. Previously, European and Han Chinese populations identified different susceptibility loci, of whi
Externí odkaz:
https://doaj.org/article/9883c49ae7774c4f91e4afbc94cb462c
Autor:
Nousheen Bibi, Asmat Ullah, Lubna Darwesh, Waqas Khan, Tanzeela Khan, Kalim Ullah, Bushra Khan, Wasim Ahmad, Umm-e-Kalsoom
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Non-syndromic oculocutaneous albinism (nsOCA) is an inherited disorder of melanin biosynthesis with autosomal recessive mode of inheritance, presenting either hypopigmented or depigmented skin, hair, and eyes. It is genetically heterogeneous with sev
Externí odkaz:
https://doaj.org/article/f29565cb3295421aa00634f71b071468
Publikováno v:
In Primary Care Diabetes February 2016 10(1):3-9