Literature DB >> 6772543

A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia.

L Pedersen, P Platz, L P Ryder, L U Lamm, J Dissing.   

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Year:  1980        PMID： 6772543     DOI： 10.1007/bf00291585

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  18 in total

1.  The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1956-06       Impact factor: 11.025

2.  HLA and disease susceptibility: a primer.

Authors:  L E Rosenberg; K K Kidd
Journal:  N Engl J Med       Date:  1977-11-10       Impact factor: 91.245

3.  Localization of the human GLO gene locus.

Authors:  B Olaisen; T Gedde-Dahl; E Thorsby
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

4.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

5.  Genetic and clinical aspects of Charcot-Marie-Tooth's disease.

Authors:  H Skre
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

6.  Spinocerebellar ataxia: study of a large kindred. I. General information and genetics.

Authors:  R D Currier; G Glover; J F Jackson; A C Tipton
Journal:  Neurology       Date:  1972-10       Impact factor: 9.910

7.  The relation of parental sex and age to recombination in the HL-A system.

Authors:  L R Weitkamp; J J Van Rood; E Thorsby; W Bias; M Fotino; S D Lawler; J Dausset; W R Mayr; J Bodmer; F E Ward; J Seignalet; R Payne; F Kissmeyer-Nielsen; R A Gatti; J A Sachs; L U Lamm
Journal:  Hum Hered       Date:  1973       Impact factor: 0.444

8.  Hereditary neurologic disorders, characterized by ataxia. Immunological in vitro parameters and HLA.

Authors:  L Pedersen; P Platz; N E Raun
Journal:  Acta Pathol Microbiol Scand C       Date:  1980-12

9.  HLA and complement typing in olivo-ponto-cerebellar atrophy.

Authors:  J P Wastiaux; G Lamoureux; J P Bouchard; A Durivage; C Barbeau; A Barbeau
Journal:  Can J Neurol Sci       Date:  1978-02       Impact factor: 2.104

10.  HLA--determination in families with hereditary ataxia.

Authors:  E Möller; B Hindfelt; J E Olsson
Journal:  Tissue Antigens       Date:  1978-11
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  14 in total

1.  Linkage studies of Friedreich ataxia by means of blood-group and protein markers.

Authors:  B J Keats; L J Ward; M Lu; S Krieger; M A Wilensky; C J Forster-Gibson; M Roy; M Monté; A Barbeau; N E Simpson
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

2.  A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance.

Authors:  J Sánchez-Corona; D García-Cruz; A González-Angulo; M C Alvarez-Arratia; R M Rodríguez; J M Cantú
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  HLA-linked and unlinked determinants of multiple sclerosis.

Authors:  H Z Ho; J L Tiwari; R W Haile; P I Terasaki; N E Morton
Journal:  Immunogenetics       Date:  1982       Impact factor: 2.846

4.  Linkage investigations in two families with hereditary ataxia.

Authors:  J Van Rossum; H Veenema; L N Went
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-06       Impact factor: 10.154

5.  The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.

Authors:  H Y Zoghbi; C Jodice; L A Sandkuijl; T J Kwiatkowski; A E McCall; S A Huntoon; P Lulli; M Spadaro; M Litt; H M Cann
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

6.  Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

Authors:  I Lopes-Cendes; E Andermann; E Attig; F Cendes; S Bosch; M Wagner; F Gerstenbrand; F Andermann; G A Rouleau
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

7.  Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

Authors:  S S Rich; P Wilkie; L Schut; G Vance; H T Orr
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

8.  Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.

Authors:  A Lunkes; S Gispert; J Enczmann; G Auburger
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

9.  Linkage between late onset, dominant spinocerebellar ataxia and HLA.

Authors:  L Werdelin; P Platz; L U Lamm
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset.

Authors:  M Spadaro; P Giunti; G B Colazza; F Naso; F Bianco; C Morocutti
Journal:  Ital J Neurol Sci       Date:  1993-01
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