Successful treatment with two siblings affected classic Bartter syndrome

por Khanh, Nguyen Ngoc, Dung, Vu Chi
Publicado 2015

Phenotype and genotype of patients with disorder of sex development due to 5α-reductase deficiency

por Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Fukami, Maki
Publicado 2015

Late-Onset Ornithine Transcarbamylase Deficiency and Variable Phenotypes in Vietnamese Females With OTC Mutations

por Nguyen, Huy-Hoang, Khanh Nguyen, Ngoc, Dung Vu, Chi, Thu Huong Nguyen, Thi, Nguyen, Ngoc-Lan
Publicado 2020

Hearing loss in osteogenesis imperfecta patients

por Ha, Lai Thu, Dung, Vu Chi, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Chau, Luong Hong
Publicado 2015

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

por Khanh, Nguyen Ngoc, Dung, Vu Chi, Thao, Bui Phuong, Ngoc, Can Thi Bich, Hoan, Nguyen Thi, Dat, Nguyen Phu
Publicado 2015

Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

por Ngoc, Can Thi Bich, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Zennaro, Maria-Christina, Wudy, Stefan A
Publicado 2015

Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

por Mai, DoThi Thanh, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu
Publicado 2015

Congenital adrenal hyperplasia with cholestatic jaundice: a case report

por Mai, DoThi Thanh, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu
Publicado 2015

Hypopituitarism due to central nervous system germinoma: a case report

por Mai, DoThi Thanh, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu
Publicado 2015

Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case

por Dung, Vu Chi, Thao, Bui Phuong, Ngoc, Can Thi Bich, Khanh, Nguyen Ngoc, Dat, Nguyen Phu, Ellard, Sian, Craig, Maria
Publicado 2015

Mutations of ABCD1 gene and phenotype of Vietnamese patients with X-linked adrenoleukodystrophy (X-ALD)

por Dung, Vu Chi, Shimozawa, Nobuyuki, Khanh, Nguyen Ngoc, Thao, Bui Phuong, Ngoc, Can Thi Bich, Dat, Nguyen Phu, Hoan, Nguyen Thi
Publicado 2013

Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families

por Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu, Hoan, Nguyen Thi, Morel, Yves
Publicado 2015

Treatment outcome and some affecting factors of congenital adrenalhyperplasia

por Dat, Nguyen Phu, Giang, Nguyen Thuy, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Hoan, Nguyen Thi
Publicado 2013

Factors affecting on the mental development in children with Congenital Hypothyroidism

por Dat, Nguyen Phu, Tra, Van Lam, Dung, Vu Chi, Thao, Bui Phuong, Ngoc, Can Thi Bich, Khanh, Nguyen Ngoc, Hoan, Nguyen Thi
Publicado 2013

Mixed embryonal carcinoma – teratoma cause early puberty: a case report

por Ngoc, Can Thi Bich, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Son, Tran Ngoc, Thach, Hoang Ngoc, Hoan, Nguyen Thi
Publicado 2015

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

por Dung, Vu Chi, Mai, Nguyen Phuong, Hoang, Nguyen Huy, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu
Publicado 2015

A case report of neonatal adrenocortical carcinoma

por Thao, Bui Phuong, Dung, Vu Chi, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Duong, Dang Anh, Son, Tran Ngoc, Thach, Hoang Ngoc
Publicado 2015

The pattern of disorders of sex development in Vietnamese children

por Nga, Pham Thu, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Nguyen Thi, Hoan, Nguyen Phu, Dat
Publicado 2015

Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia

por Huong, Ngo Thi Thu, Dat, Nguyen Phu, Hoan, Nguyen Thi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dung, Vu Chi
Publicado 2013

Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation

por Ngoc, Can Thi Bich, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dat, Nguyen Phu, Craig, Maria, Ellard, Sian, Hoan, Nguyen Thi
Publicado 2015