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J H Walter

Showing results (71-80 of 96) with videos related to

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Archives of Disease in Childhood|May 1, 1997
Prolidase deficiency and systemic lupus erythematosusM Shrinath, J H Walter, M Haeney, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Prenatal diagnosis of Canavan disease--problems and dilemmasG T Besley, O N Elpeleg, A Shaag, et al.
The Journal of Pediatrics|August 1, 1995
Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter changeM A Cleary, J H Walter, J E Wraith, et al.
Journal of Inherited Metabolic Disease|February 5, 2009
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort studyJ H Walter, A Patterson, J Till, et al.
European Journal of Pediatrics|January 1, 1989
Chronic renal failure in methylmalonic acidaemiaJ H Walter, A Michalski, W M Wilson, et al.
Journal of Inherited Metabolic Disease|July 26, 2006
Carnitine transporter defect: diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infantsS Vijay, A Patterson, S Olpin, et al.
Veterinary Microbiology|June 1, 1992
Papillomavirus associated skin lesions in a cat seropositive for feline immunodeficiency virusH F Egberink, A Berrocal, H A Bax, et al.
Lancet (London, England)|July 9, 1994
Magnetic resonance imaging of the brain in phenylketonuriaM A Cleary, J H Walter, J E Wraith, et al.
Tijdschrift Voor Diergeneeskunde|April 1, 1992
Viral papillomatosis in a catA Berrocal, T S van den Ingh, H F Egberink, et al.
Archives of Disease in Childhood|March 23, 1999
Generalised uridine diphosphate galactose-4-epimerase deficiencyJ H Walter, R E Roberts, G T Besley, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Archives of Disease in Childhood|May 1, 1997
Prolidase deficiency and systemic lupus erythematosusM Shrinath, J H Walter, M Haeney, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Prenatal diagnosis of Canavan disease--problems and dilemmasG T Besley, O N Elpeleg, A Shaag, et al.
The Journal of Pediatrics|August 1, 1995
Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter changeM A Cleary, J H Walter, J E Wraith, et al.
Journal of Inherited Metabolic Disease|February 5, 2009
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort studyJ H Walter, A Patterson, J Till, et al.
European Journal of Pediatrics|January 1, 1989
Chronic renal failure in methylmalonic acidaemiaJ H Walter, A Michalski, W M Wilson, et al.
Journal of Inherited Metabolic Disease|July 26, 2006
Carnitine transporter defect: diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infantsS Vijay, A Patterson, S Olpin, et al.
Veterinary Microbiology|June 1, 1992
Papillomavirus associated skin lesions in a cat seropositive for feline immunodeficiency virusH F Egberink, A Berrocal, H A Bax, et al.
Lancet (London, England)|July 9, 1994
Magnetic resonance imaging of the brain in phenylketonuriaM A Cleary, J H Walter, J E Wraith, et al.
Tijdschrift Voor Diergeneeskunde|April 1, 1992
Viral papillomatosis in a catA Berrocal, T S van den Ingh, H F Egberink, et al.
Archives of Disease in Childhood|March 23, 1999
Generalised uridine diphosphate galactose-4-epimerase deficiencyJ H Walter, R E Roberts, G T Besley, et al.
Pageof 10