D Stansbie|S J Wallace|C Marsac - JoVE Visualize

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Journal of Inherited Metabolic Disease|March 21, 1998

Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.

European Journal of Pediatrics|October 1, 1981

Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosisA Munnich, J M Saudubray, A Cotisson, et al.

Prenatal Diagnosis|December 11, 1999

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.

Hospital Medicine (London, England : 1998)|August 29, 1998

Epilepsy--a guide to medical treatment. 1: Antiepileptic drugsS J Wallace, C D Binnie, S W Brown, et al.

Hospital Medicine (London, England : 1998)|October 17, 1998

Epilepsy--a guide to medical treatment. 2: Non-drug aspectsS J Wallace, C D Binnie, S W Brown, et al.

Acta Paediatrica Scandinavica|January 1, 1982

Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.

Nucleic Acids Research|October 25, 1989

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndromeI Nelson, F Degoul, B Obermaier-Kusser, et al.

Archives Francaises De Pediatrie|February 1, 1981

[Multiple biotin-dependent carboxylase deficiencies (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.

The Science of the Total Environment|June 12, 2022

Structural and functional spatial dynamics of microbial communities in aerated and non-aerated horizontal flow treatment wetlandsD D Silveira, A J Farooq, S J Wallace, et al.

Ecotoxicology and Environmental Safety|December 26, 2017

Airborne polycyclic aromatic compounds contribute to the induction of the tumour-suppressing P53 pathway in wild double-crested cormorantsS J Wallace, S R de Solla, P J Thomas, et al.

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Showing results (121-130 of 147) with videos related to

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Pageof 15

Journal of Inherited Metabolic Disease|March 21, 1998

Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.

European Journal of Pediatrics|October 1, 1981

Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosisA Munnich, J M Saudubray, A Cotisson, et al.

Prenatal Diagnosis|December 11, 1999

First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.

Hospital Medicine (London, England : 1998)|August 29, 1998

Epilepsy--a guide to medical treatment. 1: Antiepileptic drugsS J Wallace, C D Binnie, S W Brown, et al.

Hospital Medicine (London, England : 1998)|October 17, 1998

Epilepsy--a guide to medical treatment. 2: Non-drug aspectsS J Wallace, C D Binnie, S W Brown, et al.

Acta Paediatrica Scandinavica|January 1, 1982

Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.

Nucleic Acids Research|October 25, 1989

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndromeI Nelson, F Degoul, B Obermaier-Kusser, et al.

Archives Francaises De Pediatrie|February 1, 1981

[Multiple biotin-dependent carboxylase deficiencies (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.

The Science of the Total Environment|June 12, 2022

Structural and functional spatial dynamics of microbial communities in aerated and non-aerated horizontal flow treatment wetlandsD D Silveira, A J Farooq, S J Wallace, et al.

Ecotoxicology and Environmental Safety|December 26, 2017

Airborne polycyclic aromatic compounds contribute to the induction of the tumour-suppressing P53 pathway in wild double-crested cormorantsS J Wallace, S R de Solla, P J Thomas, et al.

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