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C Theda

Showing results (1-10 of 8) with videos related to

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Journal of the Neurological Sciences|July 1, 1992
Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelinationC Theda, A B Moser, J M Powers, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 28, 2015
Medical and ethical challenges in the case of a prenatally undiagnosed massive congenital brain tumorM Olischar, T Stavroudis, J K Karp, et al.
The Journal of Pediatrics|May 1, 1993
Increased very long chain fatty acids in patients on a ketogenic diet: a cause of diagnostic confusionC Theda, R C Woody, S Naidu, et al.
Molecular and Cellular Biology|November 1, 1995
Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisomeJ E Kalish, C Theda, J C Morrell, et al.
Annals of Neurology|February 1, 1996
Neuronal migration abnormality in peroxisomal bifunctional enzyme defectW E Kaufmann, C Theda, S Naidu, et al.
Human Molecular Genetics|July 1, 1995
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variabilityW J Park, G A Meyers, X Li, et al.
American Journal of Human Genetics|August 1, 1995
Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.
American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of the Neurological Sciences|July 1, 1992
Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelinationC Theda, A B Moser, J M Powers, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 28, 2015
Medical and ethical challenges in the case of a prenatally undiagnosed massive congenital brain tumorM Olischar, T Stavroudis, J K Karp, et al.
The Journal of Pediatrics|May 1, 1993
Increased very long chain fatty acids in patients on a ketogenic diet: a cause of diagnostic confusionC Theda, R C Woody, S Naidu, et al.
Molecular and Cellular Biology|November 1, 1995
Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisomeJ E Kalish, C Theda, J C Morrell, et al.
Annals of Neurology|February 1, 1996
Neuronal migration abnormality in peroxisomal bifunctional enzyme defectW E Kaufmann, C Theda, S Naidu, et al.
Human Molecular Genetics|July 1, 1995
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variabilityW J Park, G A Meyers, X Li, et al.
American Journal of Human Genetics|August 1, 1995
Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.
American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.
Pageof 1