Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Rahmah Rasat"'
Autor:
Ani Amelia Zainuddin, Sonia Regina Grover, Nur Azurah Abdul Ghani, Loo Ling Wu, Rahmah Rasat, Mohd. Rizal Abdul Manaf, Khadijah Shamsuddin, Zaleha Abdullah Mahdy
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-9 (2020)
Abstract Background This study investigates the health-related quality of life (HRQOL) of female patients with congenital adrenal hyperplasia (CAH) in Malaysia. The objectives were to attain socio-demographic and medical data on these Malaysian femal
Externí odkaz:
https://doaj.org/article/fcdeed04b81e4346828426af72d05f0d
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
Publikováno v:
International Journal of Endocrinology, Vol 2017 (2017)
The aim of this study is to determine the behavioural problems of children with 46XY disorders of sex development (DSD) with genital ambiguity and to identify the risk factors that may influence behaviour. The 27 participants (aged 6–18 years) cons
Externí odkaz:
https://doaj.org/article/7cea6b5753c24e5eab6bfd1bdb931973
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
The aim of this study was to determine the behavioral outcome in children with CAH and to identify the risk factors that may influence it. Participants (aged 6–18 years) included 29 girls and 20 boys with CAH and unaffected siblings (25 girls and 1
Externí odkaz:
https://doaj.org/article/4b16f2d7245347dfa48f3b2678af3b87
Autor:
Khadijah Shamsuddin, Nur Azurah Abdul Ghani, Loo Ling Wu, Ani Amelia Zainuddin, Mohd Rizal Abdul Manaf, Rahmah Rasat, Zaleha Abdullah Mahdy, Sonia Grover
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-9 (2020)
Health and Quality of Life Outcomes
Health and Quality of Life Outcomes
Background This study investigates the health-related quality of life (HRQOL) of female patients with congenital adrenal hyperplasia (CAH) in Malaysia. The objectives were to attain socio-demographic and medical data on these Malaysian females with C
Autor:
Ani Amelia Zainuddin, Zaleha Abdullah Mahdy, Rahmah Rasat, Khadijah Shamsuddin, Abdul Ghani Na, Grover, Abdul Manaf Mr, Wu Ll
Publikováno v:
Yearbook of Paediatric Endocrinology.
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
Autor:
Syed Zulkifli Syed Zakaria, Nor Azian Abdul Murad, Nadiah Mohd Nawawi, Rahman Jamal, Yock Ping Chow, Bilkis Banu Abd Aziz, Rahmah Rasat, Zarina Abdul Latiff, Nalini M Selveindran
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 484
Background Osteogenesis imperfecta (OI) is a rare genetic bone disease characterized by bone fragility and low bone mass. OI was mainly caused by genetic mutations in collagen genes, COL1A1 and COL1A2. Nevertheless, new genes have been identified to
Publikováno v:
International Journal of Endocrinology, Vol 2017 (2017)
International Journal of Endocrinology
International Journal of Endocrinology
The aim of this study is to determine the behavioural problems of children with 46XY disorders of sex development (DSD) with genital ambiguity and to identify the risk factors that may influence behaviour. The 27 participants (aged 6–18 years) cons
Publikováno v:
Hormone research in paediatrics. 88(5)
Background/Aims: Disorders of sex development (DSD) are a heterogeneous group of rare conditions. Evidence-based treatment is challenged by a lack of clinical longitudinal outcome studies. We sought to investigate the quality of life of children with