E-LIB Suche - Ergebnisse für: Dung Vu, Chi

1

Closing the Type 1 Diabetes gap in South-East Asia through ..:

Ng, Sze May ; Malene, IV ; Nilar, Myint...
Diabetes Research and Clinical Practice. 187 (2022) - p. 109868 , 2022

Link: https://doi.org/10.1016/..

2

Genetic Etiology of Neonatal Diabetes Mellitus in Vietnames..:

Ngoc, Can Thi Bich ; Dung, Vu Chi ; De Franco, Elisa...
Frontiers in Endocrinology. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

3

Cockayne syndrome without UV-sensitivity in Vietnamese sibl..:

Duong, Nguyen Thuy ; Dinh, Tran Huu ; Möhl, Britta S....
Aging. 14 (2022) 13 - p. 5299-5310 , 2022

Link: https://doi.org/10.18632..

4

Molecular Genetics, Clinical Characteristics, and Treatment..:

Ngoc, Can Thi Bich ; Dien, Tran Minh ; De Franco, Elisa...
Frontiers in Endocrinology. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

5

A novel frameshift PHKA2 mutation in a family with glycogen..:

Nguyen, Ngoc-Lan ; Thi Bich Ngoc, Can ; Dung Vu, Chi..
Clinica Chimica Acta. 508 (2020) - p. 9-15 , 2020

Link: https://doi.org/10.1016/..

6

Late-Onset Ornithine Transcarbamylase Deficiency and Variab..:

Nguyen, Huy-Hoang ; Khanh Nguyen, Ngoc ; Dung Vu, Chi..
Frontiers in Pediatrics. 8 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

7

Diversity in the incidence and spectrum of organic acidemia..:

Shibata, Naoaki ; Hasegawa, Yuki ; Yamada, Kenji...
Molecular Genetics and Metabolism Reports. 16 (2018) - p. 5-10 , 2018

Link: https://doi.org/10.1016/..

8

Autosomal recessive Noonan syndrome associated with biallel..:

Johnston, Jennifer J. ; van der Smagt, Jasper J. ; Rosenfeld, Jill A....
Genetics in Medicine. 20 (2018) 10 - p. 1175-1185 , 2018

Link: https://doi.org/10.1038/..

9

Hematopoietic Stem Cell Transplantation for Patients with M..:

Kubaski, Francyne ; Yabe, Hiromasa ; Suzuki, Yasuyuki...
Biology of Blood and Marrow Transplantation. 23 (2017) 10 - p. 1795-1803 , 2017

Link: https://doi.org/10.1016/..

10

Glycosaminoglycan levels in dried blood spots of patients w..:

Kubaski, Francyne ; Suzuki, Yasuyuki ; Orii, Kenji...
Molecular Genetics and Metabolism. 120 (2017) 3 - p. 247-254 , 2017

Link: https://doi.org/10.1016/..

11

ID: 1048 A novel nonsense mutation in the CYP21A2 gene of a..:

Tran, Van Khanh ; Ta, Thanh Van ; Tran, Thinh Huy...
Biomedical Research and Therapy. 4 (2017) S - p. 129 , 2017

Link: https://doi.org/10.15419..

12

The clinical features of osteogenesis imperfecta in Vietnam:

Binh, Ho Duy ; Maasalu, Katre ; Dung, Vu Chi...
International Orthopaedics. 41 (2016) 1 - p. 21-29 , 2016

Link: https://doi.org/10.1007/..

13

Therapies for the bone in mucopolysaccharidoses:

Tomatsu, Shunji ; Alméciga-Díaz, Carlos J. ; Montaño, Adriana M....
Molecular Genetics and Metabolism. 114 (2015) 2 - p. 94-109 , 2015

Link: https://doi.org/10.1016/..

14

Eye and renal complication in pediatric patients with diabe..:

Hieu, Nguyen Tran Ngoc ; PhuongThao, Bui ; Dung, Vu Chi...
International Journal of Pediatric Endocrinology. 2015 (2015) S1 - p. , 2015

Link: https://doi.org/10.1186/..

15

Phenotype and genotype of patients with disorder of sex dev..:

Dung, Vu Chi ; Thao, Bui Phuong ; Khanh, Nguyen Ngoc..
International Journal of Pediatric Endocrinology. 2015 (2015) S1 - p. , 2015

Link: https://doi.org/10.1186/..