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The New England Journal of Medicine
|
June 1, 2007
Alternative-pathway therapy for hyperammonemia
Vivian E Shih
Journal of Child Neurology
|
September 15, 2006
Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency
Florian Eichler, Wen-Hann Tan, Vivian E Shih, et al.
Obstetrics and Gynecology
|
January 6, 2006
Fetal fatty acid oxidation defects and maternal liver disease in pregnancy
Marsha F Browning, Harvey L Levy, Louise E Wilkins-Haug, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 3, 2012
Long-term follow-up of four patients affected by HHH syndrome
Sook Z Kim, Wung J Song, William L Nyhan, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1
Wen-Qi Zeng, Hanlin Gao, Louise Brueton, et al.
Stroke
|
May 10, 2003
Low vitamin B6 but not homocyst(e)ine is associated with increased risk of stroke and transient ischemic attack in the era of folic acid grain fortification
Peter J Kelly, Vivian E Shih, J Philip Kistler, et al.
Journal of Inherited Metabolic Disease
|
July 11, 2006
Pericardial effusion in primary systemic carnitine deficiency
Duangrurdee Wattanasirichaigoon, Pongsak Khowsathit, Anannit Visudtibhan, et al.
Pediatrics
|
May 3, 2008
Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening
Ho-Wen Hsu, Thomas H Zytkovicz, Anne Marie Comeau, et al.
Pediatrics
|
September 6, 2005
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature
Wen-Hann Tan, Florian S Eichler, Sadaf Hoda, et al.
The Journal of Pediatrics
|
March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema
Jonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
The New England Journal of Medicine
|
June 1, 2007
Alternative-pathway therapy for hyperammonemia
Vivian E Shih
Journal of Child Neurology
|
September 15, 2006
Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency
Florian Eichler, Wen-Hann Tan, Vivian E Shih, et al.
Obstetrics and Gynecology
|
January 6, 2006
Fetal fatty acid oxidation defects and maternal liver disease in pregnancy
Marsha F Browning, Harvey L Levy, Louise E Wilkins-Haug, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 3, 2012
Long-term follow-up of four patients affected by HHH syndrome
Sook Z Kim, Wung J Song, William L Nyhan, et al.
American Journal of Medical Genetics. Part A
|
April 1, 2006
Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1
Wen-Qi Zeng, Hanlin Gao, Louise Brueton, et al.
Stroke
|
May 10, 2003
Low vitamin B6 but not homocyst(e)ine is associated with increased risk of stroke and transient ischemic attack in the era of folic acid grain fortification
Peter J Kelly, Vivian E Shih, J Philip Kistler, et al.
Journal of Inherited Metabolic Disease
|
July 11, 2006
Pericardial effusion in primary systemic carnitine deficiency
Duangrurdee Wattanasirichaigoon, Pongsak Khowsathit, Anannit Visudtibhan, et al.
Pediatrics
|
May 3, 2008
Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening
Ho-Wen Hsu, Thomas H Zytkovicz, Anne Marie Comeau, et al.
Pediatrics
|
September 6, 2005
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature
Wen-Hann Tan, Florian S Eichler, Sadaf Hoda, et al.
The Journal of Pediatrics
|
March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema
Jonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Page
of 2