Literature DB >> 1357639

Molecular biology of neurological diseases.

W J Cumming1.   

Abstract

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Year:  1992        PMID： 1357639      PMCID： PMC2399273          DOI： 10.1136/pgmj.68.798.237

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN： 0032-5473            Impact factor:   2.401


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  76 in total

1.  In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy.

Authors:  M I Evans; A Greb; L M Kunkel; A J Sacks; M P Johnson; C Boehm; H H Kazazian; E P Hoffman
Journal:  Am J Obstet Gynecol       Date:  1991-09       Impact factor: 8.661

2.  Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.

Authors:  D R Johns; J Berman
Journal:  Biochem Biophys Res Commun       Date:  1991-02-14       Impact factor: 3.575

3.  The neurofibromatosis genes: from molecular cloning to cellular function.

Authors:  A G Menon; B A Ponder; B R Seizinger
Journal:  Cancer Cells       Date:  1991-04

4.  Alzheimer's disease and the beta amyloid gene.

Authors:  P J Harrison
Journal:  BMJ       Date:  1991-06-22

5.  Polymerase chain reaction amplification from dried blood spots on Guthrie cards.

Authors:  E I Schwartz; S E Khalchitsky; R C Eisensmith; S L Woo
Journal:  Lancet       Date:  1990-09-08       Impact factor: 79.321

Review 6.  Improved diagnosis of Duchenne/Becker muscular dystrophy.

Authors:  A H Beggs; L M Kunkel
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

7.  Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.

Authors:  M R Passos-Bueno; J Terwilliger; J Ott; M Vainzof; D R Love; K E Davies; M Zatz
Journal:  Am J Med Genet       Date:  1991-01

8.  Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Authors:  F Degoul; I Nelson; P Lestienne; D Francois; N Romero; D Duboc; B Eymard; M Fardeau; G Ponsot; M Paturneau-Jouas
Journal:  J Neurol Sci       Date:  1991-02       Impact factor: 3.181

9.  Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome.

Authors:  Y Ota; M Tanaka; W Sato; K Ohno; T Yamamoto; M Maehara; T Negoro; K Watanabe; S Awaya; T Ozawa
Journal:  Invest Ophthalmol Vis Sci       Date:  1991-09       Impact factor: 4.799

10.  Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: I. Application of a new model for estimation of the risk of disease associated with the marker.

Authors:  M E Percy; V D Markovic; D R Crapper McLachlan; J M Berg; J T Hummel; M E Laing; T G Dearie; D F Andrews
Journal:  Am J Med Genet       Date:  1991-06-01
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