Hazan J - Search Results

1

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

Heinzlef O, Paternotte C, Mahieux F, Prud'homme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J. Heinzlef O, et al. Among authors: hazan j. J Med Genet. 1998 Feb;35(2):89-93. doi: 10.1136/jmg.35.2.89. J Med Genet. 1998. PMID: 9507385 Free PMC article.

2

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.

Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J. Hazan J, et al. Nat Genet. 1993 Oct;5(2):163-7. doi: 10.1038/ng1093-163. Nat Genet. 1993. PMID: 8252041

3

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B. Dürr A, et al. Among authors: hazan j. Brain. 1996 Oct;119 ( Pt 5):1487-96. doi: 10.1093/brain/119.5.1487. Brain. 1996. PMID: 8931574

4

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

Fontaine B, Davoine CS, Dürr A, Paternotte C, Feki I, Weissenbach J, Hazan J, Brice A. Fontaine B, et al. Among authors: hazan j. Am J Hum Genet. 2000 Feb;66(2):702-7. doi: 10.1086/302776. Am J Hum Genet. 2000. PMID: 10677329 Free PMC article.

5

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.

Klebe S, Durr A, Bouslam N, Grid D, Paternotte C, Depienne C, Hanein S, Bouhouche A, Elleuch N, Azzedine H, Poea-Guyon S, Forlani S, Denis E, Charon C, Hazan J, Brice A, Stevanin G. Klebe S, et al. Among authors: hazan j. Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):854-61. doi: 10.1002/ajmg.b.30518. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17503452

6

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

Vincent P, Plauchu H, Hazan J, Fauré S, Weissenbach J, Godet J. Vincent P, et al. Among authors: hazan j. Hum Mol Genet. 1995 May;4(5):945-9. doi: 10.1093/hmg/4.5.945. Hum Mol Genet. 1995. PMID: 7633456

7

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.

Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A. Bürger J, et al. Among authors: hazan j. Hum Genet. 1996 Sep;98(3):371-5. doi: 10.1007/s004390050223. Hum Genet. 1996. PMID: 8707310

8

Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy.

Vicart P, Dupret JM, Hazan J, Li Z, Gyapay G, Krishnamoorthy R, Weissenbach J, Fardeau M, Paulin D. Vicart P, et al. Among authors: hazan j. Hum Genet. 1996 Oct;98(4):422-9. doi: 10.1007/s004390050233. Hum Genet. 1996. PMID: 8792816

9

[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis].

von Fellenberg J, Paternotte C, Prud'homme JF, Weissenbach J, Hazan J, Burgunder JM. von Fellenberg J, et al. Among authors: hazan j. Schweiz Med Wochenschr. 1998 Jun 27;128(26):1043-50. Schweiz Med Wochenschr. 1998. PMID: 9700778 German.

10

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, Weissenbach J, Hazan J. Paternotte C, et al. Among authors: hazan j. Genome Res. 1998 Nov;8(11):1216-27. doi: 10.1101/gr.8.11.1216. Genome Res. 1998. PMID: 9847083 Free PMC article.

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