John West Day, MD is a Neurologist - Neuromuscular Medicine, Neurologist - General practicing in Stanford, CA
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| University | Degree | Focus | Graduated |
|---|---|---|---|
| Johns Hopkins University School of Medicine, Baltimore Md | Other Degree | 1995 |
| Institution | Focus | Year |
|---|---|---|
| Residency - Stanford University Hospital, Cardiovascular Diseases; Stanford University Hospital, Internal Medicine | Not Specified |
| Certification | Cert. Body | Year |
|---|---|---|
| Neurology Sub-Specialty: Neuromuscular Medicine | Psychiatry and Neurology | Not Specified |
| Publication | Publisher | Title | Published |
|---|---|---|---|
| Other Publication | JW Day | United Dystrophinopathy Project. LTBP4 genotype predicts age of ambulatory loss | |
| Other Publication | TURE CELL BIOLOGY | Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy | 2013 |
| Other Publication | Neuromuscular disorders | Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy | 2013 |
| Other Publication | JOURL OF NEUROLOGY | Diffusion tensor imaging reveals widespread white matter abnormalities in children | 2013 |
| Other Publication | Jourl of neurology | Diagnostic odyssey of patients with myotonic dystrophy. | |
| Other Publication | NEUROLOGY | A focal domain of extreme demethylation within D4Z4 in FSHD2 | 2013 |
| Other Publication | NEUROMUSCULAR DISORDERS | Cerebral and muscle MRI abnormalities in myotonic dystrophy | 2012 |
| Other Publication | Handbook of clinical neurology | Clinical and genetic features of spinocerebellar ataxia type 8. | 2012 |
| Other Publication | Handbook of clinical neurology | Spinocerebellar ataxia type 5. | 2012 |
| Other Publication | Anls of neurology | LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy. | |
| Other Publication | Blonsky, K., Monckton, D., Wieringa, B., Schoser, B., Day, J. W., Enge | 2010 Marigold therapeutic strategies for myotonic dystrophy. | 2012 |
| Other Publication | NEUROLOGY | Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy | 2011 |
| Other Publication | TURE STRUCTURAL & MOLECULAR BIOLOGY | Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy | 2011 |
| Other Publication | HUMAN MUTATION | Nonsense Mutation-Associated Becker Muscular Dystrophy | 2011 |
| Other Publication | NEUROMUSCULAR DISORDERS | White matter abnormalities and neurocognitive correlates | 2011 |
| Other Publication | MUSCLE & NERVE | TRAUMA, TDP-43, AND AMYOTROPHIC LATERAL SCLEROSIS | 2010 |
| Other Publication | EATING AND WEIGHT DISORDERS-STUDIES ON ANOREXIA BULIMIA AND OBESITY | Targeting parents for the treatment of pediatric obesity in boys with Duchenne muscular dystrophy | 2010 |
| Other Publication | HUMAN MUTATION | Mutatiol Spectrum of DMD Mutations in Dystrophinopathy Patients | 2009 |
| Other Publication | PLOS ONE | SNP Haplotype Mapping in a Small ALS Family | 2009 |
| Other Publication | NEUROLOGY | Congenital muscular dystrophy in a new age | 2008 |
| Other Publication | NEUROGENETICS | Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families | 2008 |
| Other Publication | JOURL OF MEDICAL GENETICS | Heterozygosity for a protein truncation mutation of sodium channel SCN8A | 2006 |
| Other Publication | HUMAN MOLECULAR GENETICS | DM2 intronic expansions | 2006 |
| Other Publication | TURE GENETICS | Spectrin mutations cause spinocerebellar ataxia type 5 | 2006 |
| Other Publication | Human genetics | Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520. | 2006 |
| Other Publication | Genome dymics | Domint non-coding repeat expansions in human disease. | 2006 |
| Other Publication | Current neurology and neuroscience reports | Genetics and molecular pathogenesis of the myotonic dystrophies. | 2005 |
| Other Publication | NEUROMUSCULAR DISORDERS | R pathogenesis of the myotonic dystrophies | 2005 |
| Other Publication | NEUROLOGY | Sudden cardiac death in myotonic dystrophy type 2 | 2004 |
| Other Publication | AMERICAN JOURL OF HUMAN GENETICS | Spinocerebellar ataxia type 8 | 2004 |
| Other Publication | AMERICAN JOURL OF HUMAN GENETICS | Myotonic dystrophy: R pathogenesis comes into focus | 2004 |
| Other Publication | NEUROLOGY | Rapid resolution of quadriplegic CIDP by combined plasmapheresis and IVIg | 2004 |
| Other Publication | AMERICAN JOURL OF HUMAN GENETICS | Myotonic dystrophy type 2: Human founder haplotype and evolutiory conservation of the repeat tract | 2003 |
| Other Publication | NEUROLOGY | Autoimmune rippling muscle | 2003 |
| Other Publication | NEUROLOGY | Myotonic dystrophy type 2 - Molecular, diagnostic and clinical spectrum | 2003 |
| Other Publication | CYTOGENETIC AND GENOME RESEARCH | Molecular genetics of spinocerebellar ataxia type 8 (SCA8) | 2003 |
| Other Publication | MUSCLE & NERVE | Randomized, controlled trial of intravenous immunoglobulin in myasthenia gravis | 2002 |
| Other Publication | Current neurology and neuroscience reports | Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2. | 2002 |
| Other Publication | MAYO CLINIC PROCEEDINGS | Force assessment in periodic paralysis after electrical muscle stimulation | 2002 |
| Other Publication | SCIENCE | Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9 | 2001 |
| Other Publication | TRANSFUSION | Clinical illness due to parvovirus B19 infection after infusion of solvent | 2000 |
| Other Publication | NEUROLOGY | Spinocerebellar ataxia type 8 - Clinical features in a large family | 2000 |
| Other Publication | HUMAN MOLECULAR GENETICS | SCA8 CTG repeat: en masse contractions in sperm and intergeneratiol sequence changes may play a | 2000 |
| Other Publication | NEUROMUSCULAR DISORDERS | Clinical and genetic characteristics of a five | 1999 |
| Other Publication | TURE GENETICS | Genetic mapping of a second myotonic dystrophy locus | 1998 |
| Other Publication | Anls of the New York Academy of Sciences | Genetic manipulation of AChR responses suggests multiple causes of weakness in slow | 1998 |
| Other Publication | TURE GENETICS | Rapid cloning of expanded trinucleotide repeat sequences from genomic D | 1998 |
| Other Publication | SYPSE | Desensitization of mutant acetylcholine receptors | 1997 |
| Other Publication | JOURL OF NEUROSCIENCE | Slow-channel transgenic mice | 1997 |
| Other Publication | JOURL OF MEDICAL ENGINEERING & TECHNOLOGY | An improved method for muscle force neuromuscular disease assessment | 1996 |
| Other Publication | MUSCLE & NERVE | Transgenic mouse model of the slow-channel syndrome | 1996 |
| Other Publication | JOURL OF NEUROSCIENCE | NICOTINIC ACETYLCHOLINE-RECEPTOR DESENSITIZATION IS REGULATED BY ACTIVATION | 1992 |
| Other Publication | ANLS OF NEUROLOGY | NORMOCALCEMIC TETANY ABOLISHED BY CALCIUM INFUSION | 1990 |
| Other Publication | LANCET | THUNDERCLAP HEADACHE - SYMPTOM OF UNRUPTURED CEREBRAL ANEURYSM | 1986 |
| Other Publication | BRAIN RESEARCH | TIME COURSE OF MINIATURE POSTSYPTIC POTENTIALS AT THE MAUTHNER FIBER GIANT SYPSE OF THE HATCHETFISH | 1985 |
| Other Publication | BRAIN RESEARCH | POSTSYPTIC CURRENTS AT THE MAUTHNER FIBER GIANT SYPSE OF THE HATCHETFISH | 1985 |
| Other Publication | BRAIN RESEARCH | POSTSYPTIC DEPRESSION OF MAUTHNER CELL-MEDIATED STARTLE REFLEX | 1980 |
John West Day, MD has not yet indicated the hospitals that he is affiliated with.
Internal Medicine
Accepts New Patients: Yes
