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Langping He

Showing results (1-10 of 82) with videos related to

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Science (New York, N.Y.)|April 25, 2015
A Chinese physics institute's defenseLangping He
Neural Networks : the Official Journal of the International Neural Network Society|October 10, 2024
Bio-inspired deep neural local acuity and focus learning for visual image recognitionLangping He, Bing Wei, Kuangrong Hao, et al.
Neuromuscular Disorders : NMD|August 19, 2003
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Reinhard Kiefer, Emma L Blakely, et al.
Neuromuscular Disorders : NMD|April 18, 2012
MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscleEmma L Blakely, Anna Butterworth, Robert D M Hadden, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Neurology. Genetics|July 27, 2018
Expanding the phenotype of de novo <i>SLC25A4</i>-linked mitochondrial disease to include mild myopathyMartin S King, Kyle Thompson, Sila Hopton, et al.
Developmental Medicine and Child Neurology|February 28, 2012
The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndromeVictoria Nesbitt, Patrick J Morrison, Ellen Crushell, et al.
Neuromuscular Disorders : NMD|September 11, 2007
The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathyRobert McFarland, Helen Swalwell, Emma L Blakely, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Maternally inherited mitochondrial DNA disease in consanguineous familiesCharlotte L Alston, Langping He, Andrew A Morris, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 31, 2007
An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRIPetr Vondracek, Marketa Hermanova, Kristina Vodickova, et al.
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Science (New York, N.Y.)|April 25, 2015
A Chinese physics institute's defenseLangping He
Neural Networks : the Official Journal of the International Neural Network Society|October 10, 2024
Bio-inspired deep neural local acuity and focus learning for visual image recognitionLangping He, Bing Wei, Kuangrong Hao, et al.
Neuromuscular Disorders : NMD|August 19, 2003
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Reinhard Kiefer, Emma L Blakely, et al.
Neuromuscular Disorders : NMD|April 18, 2012
MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscleEmma L Blakely, Anna Butterworth, Robert D M Hadden, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Neurology. Genetics|July 27, 2018
Expanding the phenotype of de novo <i>SLC25A4</i>-linked mitochondrial disease to include mild myopathyMartin S King, Kyle Thompson, Sila Hopton, et al.
Developmental Medicine and Child Neurology|February 28, 2012
The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndromeVictoria Nesbitt, Patrick J Morrison, Ellen Crushell, et al.
Neuromuscular Disorders : NMD|September 11, 2007
The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathyRobert McFarland, Helen Swalwell, Emma L Blakely, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Maternally inherited mitochondrial DNA disease in consanguineous familiesCharlotte L Alston, Langping He, Andrew A Morris, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 31, 2007
An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRIPetr Vondracek, Marketa Hermanova, Kristina Vodickova, et al.
Pageof 9