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Andrew H Crosby

Showing results (1-10 of 116) with videos related to

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The Lancet. Neurology|July 10, 2003
Disruption of cellular transport: a common cause of neurodegeneration?Andrew H Crosby
American Journal of Human Genetics|October 2, 2002
Is the transportation highway the right road for hereditary spastic paraplegia?Andrew H Crosby, Christos Proukakis
Cell Cycle (Georgetown, Tex.)|December 9, 2014
PCNA mutation affects DNA repair not replicationCatherine M Green, Emma L Baple, Andrew H Crosby
Brain : a Journal of Neurology|December 19, 2019
Lipid metabolic pathways converge in motor neuron degenerative diseasesOlivia J Rickman, Emma L Baple, Andrew H Crosby
Brain : a Journal of Neurology|October 4, 2017
Reply: PRUNE1: a disease-causing gene for secondary microcephalyEmma L Baple, Henry Houlden, Massimo Zollo, et al.
Genome|October 29, 2008
Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genesKatherine J Dick, Meriel McEntagart, Wisam Alwan, et al.
The Lancet. Neurology|August 5, 2019
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approachesSamuel Shribman, Evan Reid, Andrew H Crosby, et al.
European Journal of Medical Genetics|April 8, 2014
A novel homozygous mutation in ALS2 gene in four siblings with infantile-onset ascending hereditary spastic paralysisHatice Koçak Eker, Süleyman Ersin Unlü, Fatema Al-Salmi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 24, 2009
Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3Michael A Simpson, Harold E Cross, Leroy Cross, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorderSharon Aharoni, Gaurav Harlalka, Amaka Offiah, et al.
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
The Lancet. Neurology|July 10, 2003
Disruption of cellular transport: a common cause of neurodegeneration?Andrew H Crosby
American Journal of Human Genetics|October 2, 2002
Is the transportation highway the right road for hereditary spastic paraplegia?Andrew H Crosby, Christos Proukakis
Cell Cycle (Georgetown, Tex.)|December 9, 2014
PCNA mutation affects DNA repair not replicationCatherine M Green, Emma L Baple, Andrew H Crosby
Brain : a Journal of Neurology|December 19, 2019
Lipid metabolic pathways converge in motor neuron degenerative diseasesOlivia J Rickman, Emma L Baple, Andrew H Crosby
Brain : a Journal of Neurology|October 4, 2017
Reply: PRUNE1: a disease-causing gene for secondary microcephalyEmma L Baple, Henry Houlden, Massimo Zollo, et al.
Genome|October 29, 2008
Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genesKatherine J Dick, Meriel McEntagart, Wisam Alwan, et al.
The Lancet. Neurology|August 5, 2019
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approachesSamuel Shribman, Evan Reid, Andrew H Crosby, et al.
European Journal of Medical Genetics|April 8, 2014
A novel homozygous mutation in ALS2 gene in four siblings with infantile-onset ascending hereditary spastic paralysisHatice Koçak Eker, Süleyman Ersin Unlü, Fatema Al-Salmi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 24, 2009
Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3Michael A Simpson, Harold E Cross, Leroy Cross, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorderSharon Aharoni, Gaurav Harlalka, Amaka Offiah, et al.
Pageof 12