Literature DB >> 6069208

[Congenital muscular dystrophy].

F Vassella, M Mumenthaler, E Rossi, H Moser, U Wiesmann.   

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Year:  1967        PMID: 6069208

Source DB:  PubMed          Journal:  Dtsch Z Nervenheilkd        ISSN: 0367-004X


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  25 in total

1.  THE SIGNIFICANCE OF LACTATE DEHYDROGENASE ISOZYMES IN ABNORMAL HUMAN SKELETAL MUSCLE.

Authors:  I A BRODY
Journal:  Neurology       Date:  1964-12       Impact factor: 9.910

2.  THE DIAGNOSTIC VALUE OF SERUM CREATINE KINASE IN NEUROMUSCULAR AND MUSCULAR DISEASE.

Authors:  F VASSELLA; R RICHTERICH; E ROSSI
Journal:  Pediatrics       Date:  1965-02       Impact factor: 7.124

3.  MUSCLE LACTATE DEHYDROGENASE PATTERNS IN TWO TYPES OF X-LINKED MUSCULAR DYSTROPHY.

Authors:  C M PEARSON; N C KAR; J B PETER; T L MUNSAT
Journal:  Am J Med       Date:  1965-07       Impact factor: 4.965

4.  Congenital myopathy--A fifty-year follow-up.

Authors:  J W TURNER; F LEES
Journal:  Brain       Date:  1962-12       Impact factor: 13.501

5.  Central core disease-an investigation of a rare muscle cell abnormality.

Authors:  W K ENGEL; J B FOSTER; B P HUGHES; H E HUXLEY; R MAHLER
Journal:  Brain       Date:  1961-06       Impact factor: 13.501

6.  Arthrogryposis multiplex congenita. Case due to disease of the anterior horn cells.

Authors:  D B DRACHMAN; B Q BANKER
Journal:  Arch Neurol       Date:  1961-07

7.  Clinical pathological conference: The Children's Medical Center, Boston, Mass.

Authors:  S FARBER; J M CRAIG
Journal:  J Pediatr       Date:  1958-10       Impact factor: 4.406

8.  A new congenital non-progressive myopathy.

Authors:  K R MAGEE; G M SHY
Journal:  Brain       Date:  1956-12       Impact factor: 13.501

9.  Arthrogryposis multiplex congenita. A case of neurogenic origin.

Authors:  B Vestermark
Journal:  Acta Paediatr Scand       Date:  1966-01

10.  [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].

Authors:  S BRANDT
Journal:  Nord Med       Date:  1950-09-15
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  5 in total

1.  The rigid spine syndrome.

Authors:  E T van Munster; E M Joosten; M A van Munster-Uijtdehaage; H J Kruls; H J ter Laak
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-11       Impact factor: 10.154

2.  The syndrome of multiple ankyloses and facial anomalies. A neuropathologic analysis.

Authors:  R S Williams; L B Holmes
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

3.  Congenital muscular dystrophy, brain malformation and ocular problems (muscle, eye and brain disease) in two German families.

Authors:  R Korinthenberg; D Palm; W Schlake; J Klein
Journal:  Eur J Pediatr       Date:  1984-04       Impact factor: 3.183

Review 4.  Ullrich's congenital atonic sclerotic muscular dystrophy. A case report.

Authors:  L De Paillette; J Aicardi; F Goutières
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

5.  Congenital muscular dystrophy: brain alterations in an unselected series of Western patients.

Authors:  C P Trevisan; C Carollo; P Segalla; C Angelini; P Drigo; R Giordano
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-04       Impact factor: 10.154

  5 in total

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