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Diabetes & Metabolism
|
October 1, 1996
Mitochondrial diabetes mellitus
A Rötig, J P Bonnefont, A Munnich
Clinical Genetics
|
December 20, 2014
mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development
J Steffann, S Monnot, J-P Bonnefont
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1997
[Mitochondrial diabetes]
A Rötig, J P Bonnefont, A Munnich
Progress in Clinical and Biological Research
|
January 1, 1990
Hepatic and muscular forms of palmitoyl carnitine transferase deficiency
J P Bonnefont, I Tein, J M Saudubray, et al.
Journal of the Neurological Sciences
|
September 1, 1989
Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?
I Tein, F Demaugre, J P Bonnefont, et al.
Presse Medicale (Paris, France : 1983)
|
November 2, 1996
[Advances in genetics: what benefits children?]
S Lyonnet, J P Bonnefont, M L Briard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 1, 1996
[Rise of genetics: what are the benefits for children?]
S Lyonnet, J P Bonnefont, M L Briard, et al.
Clinical Chemistry
|
January 1, 1989
A new pitfall in plasma amino acid analysis
P Parvy, J Bardet, D Rabier, et al.
Medical Hypotheses
|
June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesis
L Faivre, J P Bonnefont, S Lyonnet, et al.
Annales De Pediatrie
|
April 1, 1984
[Association of an uncombable hair syndrome and Wilson's disease]
J Gonin, B Pepin, B Lévêque, et al.
Page
of 13
Search research articles
Search
Showing results (1-10 of 123) with videos related to
Sort By:
Page
of 13
Diabetes & Metabolism
|
October 1, 1996
Mitochondrial diabetes mellitus
A Rötig, J P Bonnefont, A Munnich
Clinical Genetics
|
December 20, 2014
mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development
J Steffann, S Monnot, J-P Bonnefont
Journees Annuelles De Diabetologie De L'Hotel-Dieu
|
January 1, 1997
[Mitochondrial diabetes]
A Rötig, J P Bonnefont, A Munnich
Progress in Clinical and Biological Research
|
January 1, 1990
Hepatic and muscular forms of palmitoyl carnitine transferase deficiency
J P Bonnefont, I Tein, J M Saudubray, et al.
Journal of the Neurological Sciences
|
September 1, 1989
Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?
I Tein, F Demaugre, J P Bonnefont, et al.
Presse Medicale (Paris, France : 1983)
|
November 2, 1996
[Advances in genetics: what benefits children?]
S Lyonnet, J P Bonnefont, M L Briard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 1, 1996
[Rise of genetics: what are the benefits for children?]
S Lyonnet, J P Bonnefont, M L Briard, et al.
Clinical Chemistry
|
January 1, 1989
A new pitfall in plasma amino acid analysis
P Parvy, J Bardet, D Rabier, et al.
Medical Hypotheses
|
June 22, 2000
Improvement of cystic fibrosis using antitumoral drugs: a hypothesis
L Faivre, J P Bonnefont, S Lyonnet, et al.
Annales De Pediatrie
|
April 1, 1984
[Association of an uncombable hair syndrome and Wilson's disease]
J Gonin, B Pepin, B Lévêque, et al.
Page
of 13