Literature DB >> 4567289

[New data on the genetics and classification of muscular dystrophies].

P E Becker.   

Abstract

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Year:  1972        PMID: 4567289

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  42 in total

1.  [PROGRESSIVE MUSCULAR DYSTROPHY. VI. INCIDENCE, CLINICAL ASPECTS AND GENETICS OF THE DUCHENNE TYPE].

Authors:  H MOSER; U WIESMANN; R RICHTERICH; E ROSSI
Journal:  Schweiz Med Wochenschr       Date:  1964-11-14

2.  Survival in x-chromosomal muscular dystrophy.

Authors:  F E DREIFUSS; G R HOGAN
Journal:  Neurology       Date:  1961-08       Impact factor: 9.910

3.  Discrimination of genetic entities in muscular dystrophy.

Authors:  C S CHUNG; N E MORTON
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

4.  Colour blindness and the Duchenne-type muscular dystrophy.

Authors:  U PHILIP; C A SMITH; J N WALTON
Journal:  Ann Hum Genet       Date:  1956-11       Impact factor: 1.670

5.  [Simple recessive form of progressive muscular dystrophy with a genealogical chart from Emmental, Switzerland].

Authors:  U PFANDLER
Journal:  Dtsch Med Wochenschr       Date:  1950-09-15       Impact factor: 0.628

6.  Studies in disorders of muscle. II Clinical manifestations and inheritance of facioscapulohumeral dystrophy in a large family.

Authors:  F H TYLER; F E STEPHENS
Journal:  Ann Intern Med       Date:  1950-04       Impact factor: 25.391

7.  [New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias].

Authors:  H W Rotthauwe; W Mortier; H Beyer
Journal:  Humangenetik       Date:  1972

8.  Genetic-epidemiological studies in progressive muscular dystrophy.

Authors:  J Prot
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

9.  Benign sex-linked muscular dystrophy. Clinical and pathological features.

Authors:  O N Markand; R R North; A N D'Agostino; D D Daly
Journal:  Neurology       Date:  1969-07       Impact factor: 9.910

10.  Unusual type of benign x-linked muscular dystrophy.

Authors:  A E Emery; F E Dreifuss
Journal:  J Neurol Neurosurg Psychiatry       Date:  1966-08       Impact factor: 10.154

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  7 in total

1.  A probable sex difference in some mutation rates.

Authors:  F Vogel
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

2.  Dominant autosomal muscular dystrophy with early contractures and cardiomyopathy (Hauptmann-Thannhauser).

Authors:  P E Becker
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

Review 3.  Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors:  H Moser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Intrafamilial variability of X-linked progressive muscular dystrophy. Mild and acute form of X-linked muscular dystrophy in the same family.

Authors:  I Hausmanowa-Petrusewicz; J Borkowska
Journal:  J Neurol       Date:  1978-04-14       Impact factor: 4.849

5.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  [Diagnostic value of muscle biopsy findings in myotonic dystrophy (Curschmann-Steinert) (author's transl)].

Authors:  D Pongratz; D Schultz; C Koppenwallner; G Hübner
Journal:  Klin Wochenschr       Date:  1979-03-01

Review 7.  The Pathogenesis and Therapies of Striated Muscle Laminopathies.

Authors:  Astrid Brull; Blanca Morales Rodriguez; Gisèle Bonne; Antoine Muchir; Anne T Bertrand
Journal:  Front Physiol       Date:  2018-10-30       Impact factor: 4.566

  7 in total

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