These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 8250534)

  • 1. Familial parkinsonism with depression: a clinicopathological study.
    Bhatia KP; Daniel SE; Marsden CD
    Ann Neurol; 1993 Dec; 34(6):842-7. PubMed ID: 8250534
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial fatal Parkinsonism with alveolar hypoventilation and mental depression.
    Purdy A; Hahn A; Barnett HJ; Bratty P; Ahmad D; Lloyd KG; McGeer EG; Perry TL
    Ann Neurol; 1979 Dec; 6(6):523-31. PubMed ID: 43704
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant Lewy body parkinsonism in a four-generation family.
    Waters CH; Miller CA
    Ann Neurol; 1994 Jan; 35(1):59-64. PubMed ID: 8285594
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A 62-year-old man with familial parkinsonism with the onset at 24 years of the age].
    Takubo H; Kondo T; Mori H; Miyake T; Suda K; Yokochi M; Imai H; Mizuno Y
    No To Shinkei; 1996 Jun; 48(6):587-97. PubMed ID: 8703564
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)--a literature review.
    Wider C; Wszolek ZK
    Parkinsonism Relat Disord; 2008; 14(1):1-7. PubMed ID: 17870652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Familial parkinsonian syndrome with athymhormia and hypoventilation].
    Lechevalier B; Schupp C; Fallet-Bianco C; Viader F; Eustache F; Chapon F; Morin P
    Rev Neurol (Paris); 1992; 148(1):39-46. PubMed ID: 1604112
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of frontotemporal dementia and parkinsonism of early onset with progressive supranuclear palsy-like features.
    Miyamoto K; Ikemoto A; Akiguchi I; Kohno R; Imura T; Fujita Y
    Clin Neuropathol; 2001; 20(1):8-12. PubMed ID: 11220696
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dominantly inherited dementia and parkinsonism, with non-Alzheimer amyloid plaques: a new neurogenetic disorder.
    Rosenberg RN; Green JB; White CL; Sparkman DR; DeArmond SJ; Kepes JJ
    Ann Neurol; 1989 Feb; 25(2):152-8. PubMed ID: 2645825
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
    Zarranz JJ; Alegre J; Gómez-Esteban JC; Lezcano E; Ros R; Ampuero I; Vidal L; Hoenicka J; Rodriguez O; Atarés B; Llorens V; Gomez Tortosa E; del Ser T; Muñoz DG; de Yebenes JG
    Ann Neurol; 2004 Feb; 55(2):164-73. PubMed ID: 14755719
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinico-pathological study of a case of familial parkinsonism with striatal degeneration.
    Sakai M; Konagaya M; Kuru S; Kato T; Matsuoka Y; Hashizume Y
    Acta Neuropathol; 2003 Jan; 105(1):76-80. PubMed ID: 12471465
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parkinsonism and extraocular motor abnormalities with unusual neuropathological findings.
    Calabrese VP; Hadfield MG
    Mov Disord; 1991; 6(3):257-60. PubMed ID: 1922131
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Autosomal recessive early-onset parkinsonism with diurnal fluctuation (AR-EPDF)--clinical characteristics].
    Yamamura Y; Kohriyama T; Kawakami H; Kaseda Y; Kuzuhara S; Nakamura S
    Rinsho Shinkeigaku; 1996 Aug; 36(8):944-50. PubMed ID: 8958746
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.
    Wszolek ZK; Gwinn-Hardy K; Wszolek EK; Muenter MD; Pfeiffer RF; Rodnitzky RL; Uitti RJ; McComb RD; Gasser T; Dickson DW
    Acta Neuropathol; 2002 Apr; 103(4):344-50. PubMed ID: 11904753
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A clinical and pathological study of a Japanese case of Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex with family history.
    Konagaya M; Kato T; Sakai M; Kuru S; Matsuoka Y; Konagaya Y; Hashizume Y; Tabira T
    J Neurol; 2003 Feb; 250(2):164-70. PubMed ID: 12574946
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic heterogeneity within a new family with the MAPT p301s mutation.
    Yasuda M; Nakamura Y; Kawamata T; Kaneyuki H; Maeda K; Komure O
    Ann Neurol; 2005 Dec; 58(6):920-8. PubMed ID: 16240366
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Early-onset parkinsonism with diurnal fluctuation--clinical and pathological studies].
    Yamamura Y; Arihiro K; Kohriyama T; Nakamura S
    Rinsho Shinkeigaku; 1993 May; 33(5):491-6. PubMed ID: 8365054
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial parkinsonism, dementia, and Lewy body disease: study of family G.
    Denson MA; Wszolek ZK; Pfeiffer RF; Wszolek EK; Paschall TM; McComb RD
    Ann Neurol; 1997 Oct; 42(4):638-43. PubMed ID: 9382476
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A 65-year-old man with Parkinsonism, gaze palsy, and dementia].
    Mizuno Y; Yokochi F; Ohta S; Mori H; Takubo H
    No To Shinkei; 1996 Apr; 48(4):381-93. PubMed ID: 8679336
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.
    Hardy J; Pérez-Tur J; Baker M; Farrer M; Crook R; Hutton M; Johnson WG; Gwinn K; Muenter M; Rocca WA; Maraganore D
    Am J Med Genet; 1998 Mar; 81(2):166-71. PubMed ID: 9613857
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
    Gasser T; Müller-Myhsok B; Wszolek ZK; Oehlmann R; Calne DB; Bonifati V; Bereznai B; Fabrizio E; Vieregge P; Horstmann RD
    Nat Genet; 1998 Mar; 18(3):262-5. PubMed ID: 9500549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.