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Results 1 - 10 of 47 for rws
  1. Romano-Ward syndrome 
    ... the condition, a situation known as reduced penetrance. RWS Ward-Romano syndrome WRS Genetic Testing Registry: Long ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  2. Horizontal gaze palsy with progressive scoliosis 
    ... al Dhalaan H, Kansu T, Stigsby B, Baloh RW. Neurologic features of horizontal gaze palsy and progressive ... TM, Salih MA, Sabatti C, Nelson SF, Baloh RW. Familial horizontal gaze palsy with progressive scoliosis maps ...
    https://medlineplus.gov/...tal-gaze-palsy-with-progressive-scoliosis - Genetics
  3. Episodic ataxia 
    ... on PubMed Central Jen J, Kim GW, Baloh RW. Clinical spectrum of episodic ataxia type 2. Neurology. ... TD, Hess EJ, Hanna MG, Griggs RC, Baloh RW; CINCH investigators. Primary episodic ataxias: diagnosis, pathogenesis and ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  4. X-linked infantile nystagmus 
    ... MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, ... L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  5. Myoclonic epilepsy with ragged-red fibers 
    ... DR, Rich P, Turnbull DM, Omer SE, Taylor RW. A new mitochondrial transfer RNAPro gene mutation associated ... nmd.2005.01.006. Citation on PubMed Taylor RW, Schaefer AM, McDonnell MT, Petty RK, Thomas AM, ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  6. Familial encephalopathy with neuroserpin inclusion bodies 
    ... on PubMed Central Davis RL, Shrimpton AE, Carrell RW, Lomas DA, Gerhard L, Baumann B, Lawrence DA, ... CM, Gooptu B, Elliott PR, Finch JT, Carrell RW, Lomas DA. Familial dementia caused by polymerization of ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  7. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... WJ, Graham BH, Scott KL, McFarland R, Taylor RW. Mutations in FBXL4 cause mitochondrial encephalopathy and a ... S, Wilichowski E, Wolf NI, Wortmann SB, Taylor RW, Mayr JA, Bonnen PE, Sperl W, Prokisch H, ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  8. Megacystis-microcolon-intestinal hypoperistalsis syndrome 
    ... RM, van der Werf CS, Sribudiani Y, Brouwer RW, van IJcken WF, Dahl N, Verheij JB, Baumann ... V, Lyu Q, Doukas M, Stoop H, Brouwer RW, van IJcken WF, Slivano OJ, Burns AJ, Christie ...
    https://medlineplus.gov/...colon-intestinal-hypoperistalsis-syndrome - Genetics
  9. Lynch syndrome 
    ... Renkonen-Sinisalo L, Hopper JL, Win AK, Haile RW, Lindor NM, Gallinger S, Le Marchand L, Newcomb ... Casey G, Gallinger S, Le Marchand L, Haile RW, Potter JD, Zheng Y, Lindor NM, Newcomb PA, ...
    https://medlineplus.gov/genetics/condition/lynch-syndrome - Genetics
  10. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... J, Jaros E, Perry RH, Schaefer AM, Taylor RW, Abdel-All Z, Lightowlers RN, Turnbull DM. Molecular ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
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