Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Fatimah Harun"'
Autor:
Ani Amelia Zainuddin, Sonia Regina Grover, Chong Hong Soon, Abdul Ghani Nur Azurah, Zaleha Abdullah Mahdy, Loo Ling Wu, Rahmah Rasat, Fatimah Harun, Wee Yan Chia, Khadijah Shamsuddin
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Girls born with congenital adrenal hyperplasia have virilized external genitalia. There is considerable debate regarding both the outcomes of feminizing genitoplasty and timing of the surgery in this population.Objective: To investigate o
Externí odkaz:
https://doaj.org/article/7d3442bfed9b4f7a97691276ac4d71e5
Autor:
Ching Chin Lee, Fatimah Harun, Muhammad Yazid Jalaludin, Choon Han Heh, Rozana Othman, Sarni Mat Junit
Publikováno v:
International Journal of Endocrinology, Vol 2013 (2013)
Congenital hypothyroidism (CH) with multinodular goiter (MNG) is uncommonly seen in children. However, CH associated with goiter is often caused by defective Thyroid peroxidase (TPO) gene. In this study, we screened for mutation(s) in the TPO gene in
Externí odkaz:
https://doaj.org/article/e8eeaffc96e44568a6f79e4ac7b428bc
Autor:
Grover, Soon Ch, Zaleha Abdullah Mahdy, asat R, Wu Ll, Ani Amelia Zainuddin, Fatimah Harun, Chia Wy, Nur Azurah Ag, Khadijah Shamsuddin
Publikováno v:
Yearbook of Paediatric Endocrinology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebc991501b25e2ead097bce55cafe8c2
https://doi.org/10.1530/ey.16.13.8
https://doi.org/10.1530/ey.16.13.8
Autor:
Khadijah Shamsuddin, Loo Ling Wu, Ani Amelia Zainuddin, Zaleha Abdullah Mahdy, Chong Hong Soon, Rahmah Rasat, Wee Yan Chia, Abdul Ghani Nur Azurah, Sonia Grover, Fatimah Harun
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Girls born with congenital adrenal hyperplasia have virilized external genitalia. There is considerable debate regarding both the outcomes of feminizing genitoplasty and timing of the surgery in this population. Objective: To investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52fb89be80107d5a5a74050497500bda
https://doi.org/10.3389/fped.2019.00144
https://doi.org/10.3389/fped.2019.00144
Autor:
Ching Chin Lee1, Fatimah Harun2, Muhammad Yazid Jalaludin2, Chor Yin Lim1, Khoon Leong Ng3, Sarni Mat Junit1 sarni@um.edu.my
Publikováno v:
BioMed Research International. 2014, Vol. 2014, p1-11. 11p.
Autor:
In Nee Kang, Fatimah Harun, Ching Chin Lee, Rozana Othman, Muhammad Yazid Jalaludin, Choon Han Heh, Sarni Mat Junit
Publikováno v:
Hormone Research in Paediatrics. 81:356-360
Background: Defects in the thyroid peroxidase (TPO) gene have been associated with goitrous congenital hypothyroidism (CH). Case Report: In this study, we report 3 siblings possessing a homozygous mutation, c.1159G>A, but exhibiting different clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73d0fc5c5ee7e8f3a9999483e0cbf8a3
https://doi.org/10.1159/000359922
https://doi.org/10.1159/000359922
Publikováno v:
Biochemical Genetics. 48:141-151
The FOXE1 gene was screened for mutations in a cohort of 34 unrelated patients with congenital hypothyroidism, 14 of whom had thyroid dysgenesis and 18 were normal (the thyroid status for 2 patients was unknown). The entire coding region of the FOXE1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4aa31aa84753b1bba9f8ce6608d5e9a
https://doi.org/10.1007/s10528-009-9306-7
https://doi.org/10.1007/s10528-009-9306-7
Publikováno v:
International Journal of Pediatric Endocrinology
Permanent Neonatal Diabetes Mellitus (PNDM) is a rare disorder where patient presents with diabetes within the first few months of life without autoantibodies associated with type 1 diabetes. The majority of PNDM cases have INS, ABCC8 or KCNJ11 mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca1a3ac9a8997c151e5bd20cbc2fad5
https://doi.org/10.1186/1687-9856-2015-s1-p29
https://doi.org/10.1186/1687-9856-2015-s1-p29
Autor:
Choon Han Heh, Rozana Othman, Muhammad Yazid Jalaludin, Ching Chin Lee, Fatimah Harun, Sarni Mat Junit
Publikováno v:
BMJ Open
Objectives The c.2268dup mutation in the thyroid peroxidase (TPO) gene is the most common TPO alteration reported in Taiwanese patients with thyroid dyshormonogenesis. The ancestors of these patients are believed to originate from the southern provin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fafbfeb6339a5c93ab64264bfd4f03a
http://europepmc.org/articles/PMC4289740
http://europepmc.org/articles/PMC4289740
Autor:
Fatimah Harun, Nurshadia Samingan, Azriyanti Anuar Zaini, Muhammad Yazid Jalaludin, Sze Lyn Jeanne Wong
Publikováno v:
Advances in Endocrinology.
Mothers are often discharged within 24 hours in most Asian countries. Therefore, our screening programs for congenital hypothyroidism (CH) must consider the value of cord blood TSH. Our objectives were to compare the incidence of CH, positive predict
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34e1b0a53f70156ecf5961540674d596