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S J Hayflick

Showing results (11-20 of 26) with videos related to

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Nature Genetics|August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndromeB Zhou, S K Westaway, B Levinson, et al.
The Journal of Investigative Dermatology|July 17, 1998
Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutationsT D Taylor, S J Hayflick, W McKinnon, et al.
Pediatric Neurology|September 12, 2001
Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndromeS J Hayflick, J M Penzien, W Michl, et al.
The Journal of Pediatrics|June 1, 1992
Cobalamin C defect associated with hemolytic-uremic syndromeM T Geraghty, E J Perlman, L S Martin, et al.
Journal of Comparative Pathology|March 18, 2006
Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophyD M Bouley, J J McIntire, B T Harris, et al.
Neurology|April 30, 2008
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulationA McNeill, D Birchall, S J Hayflick, et al.
Pediatric Neurology|September 12, 2001
hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIAB Zhou, S K Bae, A C Malone, et al.
AJNR. American Journal of Neuroradiology|September 17, 2011
Neuroimaging features of neurodegeneration with brain iron accumulationM C Kruer, N Boddaert, S A Schneider, et al.
Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.
Genomics|September 1, 1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionE W Jabs, C A Coss, S J Hayflick, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Nature Genetics|August 2, 2001
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndromeB Zhou, S K Westaway, B Levinson, et al.
The Journal of Investigative Dermatology|July 17, 1998
Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutationsT D Taylor, S J Hayflick, W McKinnon, et al.
Pediatric Neurology|September 12, 2001
Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndromeS J Hayflick, J M Penzien, W Michl, et al.
The Journal of Pediatrics|June 1, 1992
Cobalamin C defect associated with hemolytic-uremic syndromeM T Geraghty, E J Perlman, L S Martin, et al.
Journal of Comparative Pathology|March 18, 2006
Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophyD M Bouley, J J McIntire, B T Harris, et al.
Neurology|April 30, 2008
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulationA McNeill, D Birchall, S J Hayflick, et al.
Pediatric Neurology|September 12, 2001
hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIAB Zhou, S K Bae, A C Malone, et al.
AJNR. American Journal of Neuroradiology|September 17, 2011
Neuroimaging features of neurodegeneration with brain iron accumulationM C Kruer, N Boddaert, S A Schneider, et al.
Neurogenetics|October 22, 2005
A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effectP Rump, H H Lemmink, C C Verschuuren-Bemelmans, et al.
Genomics|September 1, 1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionE W Jabs, C A Coss, S J Hayflick, et al.
Pageof 3