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12 Possible Causes for bricka

  • Autosomal Recessive Spastic Paraplegia Type 72

    Accession #Hs0516 Hum Genet , 118 (6) , 785 PubMed 17297722 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hm0554 Hum Genet , 118 (6) , 782 PubMed 17297710 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hs0515 Hum Genet , 118 (6) , 785 PubMed 17297721 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no]

  • Autosomal Recessive Spastic Paraplegia Type 44

    Accession #Hs0516 Hum Genet , 118 (6) , 785 PubMed 17297722 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hm0554 Hum Genet , 118 (6) , 782 PubMed 17297710 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hs0515 Hum Genet , 118 (6) , 785 PubMed 17297721 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no]

  • Autosomal Recessive Spastic Paraplegia Type 14

    Accession #Hs0516 Hum Genet , 118 (6) , 785 PubMed 17297722 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hm0554 Hum Genet , 118 (6) , 782 PubMed 17297710 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hs0515 Hum Genet , 118 (6) , 785 PubMed 17297721 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no]

  • Autosomal Recessive Spastic Paraplegia Type 61

    Accession #Hs0516 Hum Genet , 118 (6) , 785 PubMed 17297722 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hm0554 Hum Genet , 118 (6) , 782 PubMed 17297710 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] Accession #Hs0515 Hum Genet , 118 (6) , 785 PubMed 17297721 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no]

  • Chelating Agent

    Bricka, R., and C. Williford, L. Jones (1994) “Heavy metal soil contamination at U.S.[link.springer.com] .; Bricka, R.; Chao, A.; Environ. Prog . 1997 , 16 , 274. [ Links ] 37.[scielo.br]

  • Amyotrophic Lateral Sclerosis 10

    […] mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations Stéphanie Millecamps 1 , François Salachas 2 , Cécile Cazeneuve 3 , Paul Gordon 2 , Bernard Bricka[jmg.bmj.com]

  • Autosomal Recessive Spastic Paraplegia Type 39

    Accession #Hs0516 Hum Genet , 118 (6) , 785 PubMed 17297722 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no] View Article PubMed PubMed Central Google Scholar Depienne C, Tallaksen C, Lephay JY, Bricka B, Poea-Guyon S, Fontaine B, Labauge P, Brice A, Durr A: Spastin mutations are[bmcmedgenet.biomedcentral.com] Accession #Hm0554 Hum Genet , 118 (6) , 782 PubMed 17297710 Depienne C , Tallaksen C , Lephay JY , Bricka B , Poea-Guyon S , Fontaine B , Labauge P , Brice A , Durr A (2006[ous-research.no]

  • Autosomal Dominant Spastic Paraplegia Type 4

    ., Bricka B. et al. Mutation spectrum and clinical features pf SPG4 HSP. Eur J Hum Genet 2007; 15: Suppl 1: 90. Depienne C., Fedirko E., Faucheux J. et al.[mediasphera.ru] Google Scholar Depienne C, Tallaksen C, Lephay JY, Bricka B, Poea-Guyon S, Fontaine B, et al: Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum[bmcneurol.biomedcentral.com] View Article PubMed PubMed Central Google Scholar Depienne C, Tallaksen C, Lephay JY, Bricka B, Poea-Guyon S, Fontaine B, Labauge P, Brice A, Durr A: Spastin mutations are[bmcmedgenet.biomedcentral.com]

  • Autosomal Recessive Spastic Paraplegia Type 30

    View Article PubMed PubMed Central Google Scholar Depienne C, Tallaksen C, Lephay JY, Bricka B, Poea-Guyon S, Fontaine B, Labauge P, Brice A, Durr A: Spastin mutations are[bmcmedgenet.biomedcentral.com]

  • Autosomal Dominant Spastic Paraplegia Type 31

    Depienne C, Tallaksen C, Lephay JY, Bricka B, Poea-Guyon S, Fontaine B, et al.[synapse.koreamed.org]

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