PariMarieYoungMD

PubMed

• Cognitive impairment in HIV infection is associated with MRI and CSF pattern of neurodegeneration.
  Steinbrink F, Evers S, Buerke B, Young P, Arendt G, Koutsilieri E, Reichelt D, Lohmann H, Husstedt I> ;Eur. J. Neurol.. 2013-03-01
• Neuroimaging in Susac's syndrome: focus on DTI.
  Kleffner I, Deppe M, Mohammadi S, Schwindt W, Sommer J, Young P, Ringelstein EB> ;J. Neurol. Sci.. 2010-12-15
• 1 citations
  A family with combined mutations of the hemophilia A and X-linked adrenoleukodystrophy genes
  Brent L. Fogel, Pari Young, Arthur R. Thompson, Susan Perlman> ;Neurogenetics. 2008 Jul 1
• Diffusion tensor imaging demonstrates fiber impairment in Susac syndrome.
  Kleffner I, Deppe M, Mohammadi S, Schiffbauer H, Stupp N, Lohmann H, Young P, Ringelstein EB> ;Neurology. 2008-05-06
• Treatment for Charcot-Marie-Tooth disease.
  Young P, De Jonghe P, Stögbauer F, Butterfass-Bahloul T> ;Cochrane Database Syst Rev. 2008-01-23
• Comorbidity of migraine and restless legs syndrome--a case-control study.
  Rhode AM, Hösing VG, Happe S, Biehl K, Young P, Evers S> ;Cephalalgia. 2007-11-01
• Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.
  Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V...> ;Neurology. 2004-06-22
• The causes of Charcot-Marie-Tooth disease.
  Young P, Suter U> ;Cell. Mol. Life Sci.. 2003-12-01
• Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A.
  Sancho S, Young P, Suter U> ;Brain. 2001-11-01
• Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.
  Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F> ;J. Neurol.. 2001-10-01
• Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies.
  Ørstavik K, Skard Heier M, Young P, Stögbauer F> ;Muscle Nerve. 2001-08-01
• Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity.
  Young P, Grote K, Kuhlenbäumer G, Debus O, Kurlemann H, Halfter H, Funke H, Ringelstein EB, Stögbauer F> ;J. Neurol.. 2001-05-01
• Cellular and humoral immune response in progressive multifocal leukoencephalopathy.
  Weber F, Goldmann C, Krämer M, Kaup FJ, Pickhardt M, Young P, Petry H, Weber T, Lüke W> ;Ann. Neurol.. 2001-05-01
• PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A.
  Young P, Stögbauer F, Wiebusch H, Löfgren A, Timmerman V, Van Broeckhoven C, Ringelstein EB, Assmann G, Funke H> ;Neurology. 1998-03-01
• A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.
  Young P, Wiebusch H, Stögbauer F, Ringelstein B, Assmann G, Funke H> ;Neurology. 1997-02-01
• Using restraint.
  Young P> ;Nurs Elder. 1992-01-01
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