Pesquisas alternativas:
daily compared » early compared (Expandir a Pesquisa), elderly compared (Expandir a Pesquisa)
company case » company based (Expandir a Pesquisa), company a (Expandir a Pesquisa)
book company » food company (Expandir a Pesquisa), stock company (Expandir a Pesquisa), kodak company (Expandir a Pesquisa)
compared a » compared _ (Expandir a Pesquisa), compare a (Expandir a Pesquisa), compare _ (Expandir a Pesquisa)
a company » _ company (Expandir a Pesquisa)
case ngoc » can ngoc (Expandir a Pesquisa), cao ngoc (Expandir a Pesquisa), case non (Expandir a Pesquisa)
case new » cases new (Expandir a Pesquisa), cause new (Expandir a Pesquisa), caste new (Expandir a Pesquisa)
2 daily » _ daily (Expandir a Pesquisa), a daily (Expandir a Pesquisa), 2 dairy (Expandir a Pesquisa)
a now » a new (Expandir a Pesquisa), a non (Expandir a Pesquisa), _ now (Expandir a Pesquisa)
daily compared » early compared (Expandir a Pesquisa), elderly compared (Expandir a Pesquisa)
company case » company based (Expandir a Pesquisa), company a (Expandir a Pesquisa)
book company » food company (Expandir a Pesquisa), stock company (Expandir a Pesquisa), kodak company (Expandir a Pesquisa)
compared a » compared _ (Expandir a Pesquisa), compare a (Expandir a Pesquisa), compare _ (Expandir a Pesquisa)
a company » _ company (Expandir a Pesquisa)
case ngoc » can ngoc (Expandir a Pesquisa), cao ngoc (Expandir a Pesquisa), case non (Expandir a Pesquisa)
case new » cases new (Expandir a Pesquisa), cause new (Expandir a Pesquisa), caste new (Expandir a Pesquisa)
2 daily » _ daily (Expandir a Pesquisa), a daily (Expandir a Pesquisa), 2 dairy (Expandir a Pesquisa)
a now » a new (Expandir a Pesquisa), a non (Expandir a Pesquisa), _ now (Expandir a Pesquisa)
1
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Bui, Thao Phuong, Nguyen, Khanh Ngoc, Zennaro, Maria-Christina, Wudy, Stefan A.
Publicado no Ann Transl Med (2015)
“...BACKGROUND: Pseudohypoaldosteronism type 1 (PHA1) is a rare inherited disease characterized...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
2
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Le, Hang Thi Thuy, Nguyen, Khanh Ngoc, Bui, Huong Thi
Publicado no Ann Transl Med (2015)
“...BACKGROUND AND OBJECTIVE: Mucopolysaccharidosis I (MPS I) is a rare, recessively inherited...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
3
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Le, Hang Thi Thuy, Nguyen, Khanh Ngoc, Bui, Huong Thi
Publicado no Ann Transl Med (2015)
“...BACKGROUND AND OBJECTIVE: Mucopolysaccharidosis (MPS) type II (Hunter syndrome) is an X-linked...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
4
Por Dung, Vu Chi, Thao, Bui Phuong, Ngoc, Can Thi Bich, Khanh, Nguyen Ngoc, Ellard, Sian
Publicado no Ann Transl Med (2015)
“...Maturity-onset diabetes of the young type 5 (MODY5), a type of dominantly inherited diabetes...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
5
Por Nguyen, Khanh Ngoc, Vu, Dung Chi, Can, Ngoc Thi Bich, Bui, Thao Phuong, Nguyen, Mai Chi, Yamaguchi, Seiji
Publicado no Ann Transl Med (2015)
“... and kidney disturbances and mental retardation. Case report: the 2.5 months old girl admitted with chief...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
6
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Bui, Thao Phuong, Nguyen, Khanh Ngoc
Publicado no Ann Transl Med (2015)
“...BACKGROUND AND OBJECTIVE: Osteogenesis imperfecta (OI) comprises a group of disorders principally...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
7
Por Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Fukami, Maki
Publicado no Ann Transl Med (2015)
“.... We identified mutations of SRD5A2 gene in two cases. The first case presented with isolated...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
8
Por Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Morel, Yves
Publicado no Ann Transl Med (2015)
“...) deficiency is a rare cause of CAH caused by inactivating mutations in the HSD3B2 gene. Most mutations...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
9
Por Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Publicado no Ann Transl Med (2015)
“.... Mutation HNF4A gene found 1/68 cases (1.47%). A boy born large for gestational age (birth weight 4,700 g...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
10
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Bui, Thao Phuong, Nguyen, Khanh Ngoc, Hwu, Wuh-Liang
Publicado no Ann Transl Med (2015)
“...BACKGROUND: I-cell disease (Mucolipidosis II) is a rare lysosomal storage disorder caused...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
11
Por Nguyen, Khanh Ngoc, Vu, Dung Chi, Bui, Thao Phuong, Can, Ngoc Thi Bich, Nguyen, Hoan Thi, Nguyen, Dat Phu
Publicado no Ann Transl Med (2015)
“...), “creamy” blood (21 cases). Twenty cases were asymptomatic. A total of 8/28 patients had family history...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
12
Por Nguyen, Khanh Ngoc, Vu, Dung Chi, Can, Ngoc Thi Bich, Bui, Thao Phuong, Nguyen, Mai Chi, Yamaguchi, Seiji
Publicado no Ann Transl Med (2015)
“... acidosis (PH: 7.2-7.3) in 3 cases, thrombopenia in 3 cases; ketonuria in 3 cases and hyperammonemia in 3...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
13
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Flanagan, Sarah, Ellard, Sian
Publicado no Ann Transl Med (2015)
“..., BE of −8 mmoL/L, blood glucose 42.46 mmoL/L, HbA1C 6.5%, total bilirubin 59.2 µmoL/L, direct bilirubin 29.7...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
14
Por Vu, Dinh Quang, Van Nguyen, Thi Hong, Phung, Tuyet Lan, Tran, Ngoc Son, Le, Dinh Cong, Hoang, Ngoc Thach, Tran, Tran Thi Chi Mai, Nguyen, Xuan Huy, Ngo, Diem Ngoc
Publicado no Ann Transl Med (2015)
“...) and 67% (>18 months). The favorable and unfavorable histology cases show a different frequency of MYCN...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
15
Por Thao, Bui Phuong, Dung, Vu Chi, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Hoan, Nguyen Thi, Phuong, Nguyen Thi
Publicado no Ann Transl Med (2015)
“...BACKGROUND: Turner syndrome is a relatively common chromosomal disorder. The disease affects only...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
16
Por Nguyen, Khanh Ngoc, Vu, Dung Chi, Fukao, Toshiyuki, Bui, Thao Phuong, Can, Ngoc Thi Bich, Nguyen, Hoan Thi, Yamaguchi, Seiji
Publicado no Ann Transl Med (2015)
“... Hospital of Pediatrics-Hanoi-Vietnam from 2005 to 2012. A total of 21 cases from 19 families were analyzed...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
17
Por Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Publicado no Ann Transl Med (2015)
“.... METHODS: A prospective study was conducted on 68 cases with HI diagnosed and treated in National Hospital...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
18
Por Duong, Dang Anh, Dung, Vu Chi, Dat, Nguyen Phu, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Dien, Tran Minh
Publicado no Ann Transl Med (2015)
“... are 214.2±190.6 pmol/L and 1.78±1.5 nmol/L. Gene mutations were detected in 64.29% of cases including...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
19
Por Can, Ngoc Thi Bich, Vu, Dung Chi, Bui, Thao Phuong, Nguyen, Khanh Ngoc, Nguyen, Dat Phu, Craig, Maria, Ellard, Sian, Nguyen, Hoan Thi
Publicado no Ann Transl Med (2015)
“...T > A; C43S) in exon 2 in one case; heterozygous for a splicing mutation c.188-31G > A in intron 2...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo
20
Por Dung, Vu Chi, Fukami, Maki, Ngoc, Can Thi Bich, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Nga, Pham Thu, Dat, Nguyen Phu, Ogata, Tsutomu
Publicado no Ann Transl Med (2015)
“... female partial AIS phenotype. Four cases had two labial testes, six cases had inguinal testes and two...”Publicado no Ann Transl Med (2015)
Obter o texto integral
Obter o texto integral
Artigo