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P L Marsh

Showing results (1-10 of 13) with videos related to

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European Journal of Human Genetics : EJHG|August 10, 2018
CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63Ashley P L Marsh, Gaia Novarino, Paul J Lockhart, et al.
Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|December 1, 1995
Ascent rate, post-dive exercise, and decompression sickness in the ratG W Pollard, P L Marsh, C E Fife, et al.
JCO Precision Oncology|August 27, 2025
Association of <i>RPS20</i> Loss-of-Function Variants With Colorectal Cancer Risk in a Cohort of Over 950,000 IndividualsJennifer Herrera-Mullar, Cassidy Carraway, Ashley P L Marsh, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Neurology|April 17, 2015
Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTORRichard J Leventer, Thomas Scerri, Ashley P L Marsh, et al.
Neurology. Genetics|April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 lossAshley P L Marsh, Vesna Lukic, Kate Pope, et al.
Cell Reports|February 2, 2018
DCC Is Required for the Development of Nociceptive Topognosis in Mice and HumansRonan V da Silva, Helge C Johannssen, Matthias T Wyss, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.
Journal of Neurochemistry|July 19, 2019
The energetic brain - A review from students to studentsMelina Paula Bordone, Mootaz M Salman, Haley E Titus, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|August 10, 2018
CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63Ashley P L Marsh, Gaia Novarino, Paul J Lockhart, et al.
Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|December 1, 1995
Ascent rate, post-dive exercise, and decompression sickness in the ratG W Pollard, P L Marsh, C E Fife, et al.
JCO Precision Oncology|August 27, 2025
Association of <i>RPS20</i> Loss-of-Function Variants With Colorectal Cancer Risk in a Cohort of Over 950,000 IndividualsJennifer Herrera-Mullar, Cassidy Carraway, Ashley P L Marsh, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Neurology|April 17, 2015
Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTORRichard J Leventer, Thomas Scerri, Ashley P L Marsh, et al.
Neurology. Genetics|April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 lossAshley P L Marsh, Vesna Lukic, Kate Pope, et al.
Cell Reports|February 2, 2018
DCC Is Required for the Development of Nociceptive Topognosis in Mice and HumansRonan V da Silva, Helge C Johannssen, Matthias T Wyss, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.
Journal of Neurochemistry|July 19, 2019
The energetic brain - A review from students to studentsMelina Paula Bordone, Mootaz M Salman, Haley E Titus, et al.
Pageof 2