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 *

102 related articles for article (PubMed ID: 17582979)

  • 41. Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.
    Bouhouche A; Benomar A; Bouslam N; Chkili T; Yahyaoui M
    J Med Genet; 2006 May; 43(5):441-3. PubMed ID: 16399879
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred.
    Lin P; Mao F; Liu Q; Shao C; Yan C; Gong Y
    Prenat Diagn; 2010 May; 30(5):485-6. PubMed ID: 20306460
    [No Abstract]   [Full Text] [Related]  

  • 43. [Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update].
    Wang ZZ; Cen ZD; Luo W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):429-34. PubMed ID: 23926010
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.
    Inan B; Azman F; Aktas D; Yildiz Y; Saygi S
    Acta Neurol Belg; 2023 Oct; 123(5):1985-1987. PubMed ID: 35789476
    [No Abstract]   [Full Text] [Related]  

  • 45. [Infantile spastic paraplegia in two cases from a pedigree].
    Zhang Y; Xu Y; Zhou H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):750. PubMed ID: 26419003
    [No Abstract]   [Full Text] [Related]  

  • 46. Childhood-Onset Writer's Cramp in Hereditary Spastic Paraplegia Type 15.
    Moura J; Sardoeira A; Oliveira J; Mendes A; Barros J; Sequeiros J; Barbot C; Damásio J
    Can J Neurol Sci; 2023 May; 50(3):469-471. PubMed ID: 35538608
    [No Abstract]   [Full Text] [Related]  

  • 47. A case of a rare association of spastic paraplegia and type III syndactyly.
    Colazza GB; Di Gennaro G; Quarato PP; Buzzi MG; Sabatini U
    Eur J Neurol; 2002 Jan; 9(1):105-7. PubMed ID: 11784386
    [No Abstract]   [Full Text] [Related]  

  • 48. Hereditary spastic paraplegia and Evans's syndrome.
    Ahmed FE; Qureshi IM; Wooldridge MA; Pejaver RK
    Acta Paediatr; 1996 Jul; 85(7):879-81. PubMed ID: 8819560
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Familial spastic paraplegia with peroneal amyotrophy. A family with hypersensitivity to pyrexia.
    Serena M; Rizzuto N; Moretto G; Arrigoni G
    Ital J Neurol Sci; 1990 Dec; 11(6):583-8. PubMed ID: 2081683
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Hereditary spastic paraplegia----a pedigree with five cases].
    Ning P; An R; Xu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):777. PubMed ID: 28981953
    [No Abstract]   [Full Text] [Related]  

  • 51. Severe hypodontia in association with Klinefelter (47 XXY) syndrome. A case report.
    Rock WP; McLellan NJ
    Br J Orthod; 1990 Nov; 17(4):321-3. PubMed ID: 2285702
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Familial case of May-Hegglin anomaly associated with familial spastic paraplegia.
    Fujita Y; Fujii T; Nishio A; Tuboi K; Tsuji K; Nakamura M
    Am J Hematol; 1990 Nov; 35(3):219-21. PubMed ID: 2171328
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Clinical variability and L-Dopa responsive Parkinsonism in hereditary spastic paraplegia 11.
    Everett CM; Kara E; Maresh KE; Houlden H
    J Neurol; 2012 Dec; 259(12):2726-8. PubMed ID: 22893306
    [No Abstract]   [Full Text] [Related]  

  • 54. Two siblings with mental retardation and progressive spasticity.
    Nicolaides P; Baraitser M; Brett EM
    Clin Genet; 1993 Jun; 43(6):312-4. PubMed ID: 8370152
    [No Abstract]   [Full Text] [Related]  

  • 55. A case of hereditary spastic paraplegia with demyelinating polyneuropathy.
    Beligaswatte AM; Bandusena S; Riffsy MT; Gunasekera S; Wijesekera JC
    Ceylon Med J; 2005 Sep; 50(3):128-9. PubMed ID: 16252580
    [No Abstract]   [Full Text] [Related]  

  • 56. Homozygous B4GALNT1 mutation and biochemical glutaric acidemia type II: A case report.
    Rose L; Hall K; Tang S; Hasadsri L; Kimonis V
    Clin Neurol Neurosurg; 2020 Feb; 189():105553. PubMed ID: 31812852
    [No Abstract]   [Full Text] [Related]  

  • 57. Hereditary spastic paraplegia type 8: Neuropathological findings.
    Pehrson C; Hertz JM; Wirenfeldt M; Stenager E; Wermuth L; Winther Kristensen B
    Brain Pathol; 2018 Mar; 28(2):292-294. PubMed ID: 28181327
    [No Abstract]   [Full Text] [Related]  

  • 58. Clinical Reasoning: A 28-year-old woman with lower extremity spasticity and microcytic anemia.
    Bonda C; Sharma P; LaFaver K
    Neurology; 2015 Jul; 85(2):e11-4. PubMed ID: 26170404
    [No Abstract]   [Full Text] [Related]  

  • 59. Enigma of tropical spastic paraplegia.
    Gourie-Devi M
    Neurol India; 2020; 68(2):268-269. PubMed ID: 32415001
    [No Abstract]   [Full Text] [Related]  

  • 60. The importance of understanding gait features in hereditary spastic paraplegia: accomplishments and next steps.
    Ounpuu S
    Dev Med Child Neurol; 2016 Aug; 58(8):790-1. PubMed ID: 26946256
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.