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Journal of Structural Biology
|
May 13, 2008
Detection and imaging of non-contractile inclusions and sarcomeric anomalies in skeletal muscle by second harmonic generation combined with two-photon excited fluorescence
E Ralston, B Swaim, M Czapiga, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
August 6, 2000
3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: report of one case
C Lee, F J Tsai, J Y Wu, et al.
Bone Marrow Transplantation
|
August 6, 1999
Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation
Y S Hsu, W L Hwu, S F Huang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
July 27, 2000
Molecular diagnosis of Apert syndrome in Chinese patients
F J Tsai, C H Tsai, C T Peng, et al.
Molecular Genetics and Metabolism Reports
|
March 25, 2021
Evaluation of 3-<i>O</i>-methyldopa as a biomarker for aromatic L-amino acid decarboxylase deficiency in 7 Brazilian cases
Francyne Kubaski, Zackary M Herbst, Danilo A A Pereira, et al.
Molecular Genetics and Metabolism Reports
|
January 18, 2024
Corrigendum to "Evaluation of 3-O-methyldopa as a biomarker for aromatic L-amino acid decarboxylase deficiency in 7 Brazilian cases" [27/100744/2021/ pages: 1-4]
Francyne Kubaski, Zackary M Herbst, Danilo A A Pereira, et al.
Journal of Inherited Metabolic Disease
|
March 28, 2002
Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations
Y H Chien, S C Chiang, A Huang, et al.
Journal of Inherited Metabolic Disease
|
April 6, 2012
Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C
Y H Chien, S F Peng, C C Yang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 24, 2006
Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype
M Chen, W-L Hwu, S-J Kuo, et al.
American Journal of Human Genetics
|
March 7, 2001
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency
B A Binzak, R A Wevers, S H Moolenaar, et al.
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Search research articles
Search
Showing results (61-70 of 77) with videos related to
Sort By:
Page
of 8
Journal of Structural Biology
|
May 13, 2008
Detection and imaging of non-contractile inclusions and sarcomeric anomalies in skeletal muscle by second harmonic generation combined with two-photon excited fluorescence
E Ralston, B Swaim, M Czapiga, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
August 6, 2000
3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: report of one case
C Lee, F J Tsai, J Y Wu, et al.
Bone Marrow Transplantation
|
August 6, 1999
Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation
Y S Hsu, W L Hwu, S F Huang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
July 27, 2000
Molecular diagnosis of Apert syndrome in Chinese patients
F J Tsai, C H Tsai, C T Peng, et al.
Molecular Genetics and Metabolism Reports
|
March 25, 2021
Evaluation of 3-<i>O</i>-methyldopa as a biomarker for aromatic L-amino acid decarboxylase deficiency in 7 Brazilian cases
Francyne Kubaski, Zackary M Herbst, Danilo A A Pereira, et al.
Molecular Genetics and Metabolism Reports
|
January 18, 2024
Corrigendum to "Evaluation of 3-O-methyldopa as a biomarker for aromatic L-amino acid decarboxylase deficiency in 7 Brazilian cases" [27/100744/2021/ pages: 1-4]
Francyne Kubaski, Zackary M Herbst, Danilo A A Pereira, et al.
Journal of Inherited Metabolic Disease
|
March 28, 2002
Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations
Y H Chien, S C Chiang, A Huang, et al.
Journal of Inherited Metabolic Disease
|
April 6, 2012
Long-term efficacy of miglustat in paediatric patients with Niemann-Pick disease type C
Y H Chien, S F Peng, C C Yang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 24, 2006
Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype
M Chen, W-L Hwu, S-J Kuo, et al.
American Journal of Human Genetics
|
March 7, 2001
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency
B A Binzak, R A Wevers, S H Moolenaar, et al.
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