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Results 1 - 10 of 234 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. RRM2B gene 
    ... PF, Horvath R, Turnbull DM, Gorman GS, Taylor RW. RRM2B mutations are frequent in familial PEO with ... on PubMed Central Lim AZ, McFarland R, Taylor RW, Gorman GS. RRM2B Mitochondrial DNA Maintenance Defects. 2014 ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  7. Pleural Fluid Analysis: MedlinePlus Medical Test 
    ... nih.gov/books/NBK448189/#_article-20929_s3_ Light RW. The Light Criteria. Clin Chest Med [Internet]. 2013 ... nih.gov/health/pleural-disorders Porcel JM, Light RW. Diagnostic Approach to Pleural Effusion in Adults. Am ...
    https://medlineplus.gov/lab-tests/pleural-fluid-analysis - Medical Tests
  8. 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
  9. 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
  10. MT-ND1 gene 
    ... C, Ketteridge D, Turnbull DM, Thorburn DR, Taylor RW. Mutations of the mitochondrial ND1 gene as a ... PubMed Mitchell AL, Elson JL, Howell N, Taylor RW, Turnbull DM. Sequence variation in mitochondrial complex I ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
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