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F Rocchiccioli

Showing results (41-50 of 56) with videos related to

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Neuropediatrics|August 1, 1986
Neurological deterioration and lactic acidemia in biotinidase deficiency. A treatable condition mimicking Leigh's diseaseG Mitchell, H Ogier, A Munnich, et al.
Lancet (London, England)|May 14, 1983
Antenatal diagnosis of glutaricaciduria type IIG Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1988
Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosisB Boutin, M C Routon, F Rocchiccioli, et al.
Biochimica Et Biophysica Acta|February 19, 1988
A new human pathology with visceral accumulation of long-chain n-alkanes; tissue distribution of the stored compounds and pathophysiological hypothesesR Salvayre, A Nègre, F Rocchiccioli, et al.
International Journal of Systematic Bacteriology|October 23, 1997
Thermotoga hypogea sp. nov., a xylanolytic, thermophilic bacterium from an oil-producing wellM L Fardeau, B Ollivier, B K Patel, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patientsR J Wanders, L Ijlst, M Duran, et al.
Pediatric Research|December 1, 1990
Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhoodF Rocchiccioli, R J Wanders, P Aubourg, et al.
Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Etiological diagnosis of primary adrenal insufficiency using an original flowchart of immune and biochemical markersS Laureti, P Aubourg, F Calcinaro, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Neuropediatrics|August 1, 1986
Neurological deterioration and lactic acidemia in biotinidase deficiency. A treatable condition mimicking Leigh's diseaseG Mitchell, H Ogier, A Munnich, et al.
Lancet (London, England)|May 14, 1983
Antenatal diagnosis of glutaricaciduria type IIG Mitchell, J M Saudubray, Y Benoit, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1988
Peripheral neuropathy associated with erythrophagocytic lymphohistiocytosisB Boutin, M C Routon, F Rocchiccioli, et al.
Biochimica Et Biophysica Acta|February 19, 1988
A new human pathology with visceral accumulation of long-chain n-alkanes; tissue distribution of the stored compounds and pathophysiological hypothesesR Salvayre, A Nègre, F Rocchiccioli, et al.
International Journal of Systematic Bacteriology|October 23, 1997
Thermotoga hypogea sp. nov., a xylanolytic, thermophilic bacterium from an oil-producing wellM L Fardeau, B Ollivier, B K Patel, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patientsR J Wanders, L Ijlst, M Duran, et al.
Pediatric Research|December 1, 1990
Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhoodF Rocchiccioli, R J Wanders, P Aubourg, et al.
Revue Neurologique|June 1, 1996
[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies]P Laforêt, B Eymard, A Lombès, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Etiological diagnosis of primary adrenal insufficiency using an original flowchart of immune and biochemical markersS Laureti, P Aubourg, F Calcinaro, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Pageof 6