Literature DB >> 13938944

Sudanophil leucodystrophy in a pachygyric brain.

R M NORMAN, A H TINGEY, J C VALENTINE, T A DANBY.   

Abstract

Keywords:  CEREBRAL SCLEROSIS, DIFFUSE; MICROCEPHALY

Mesh:

Year:  1962        PMID: 13938944      PMCID: PMC495493          DOI: 10.1136/jnnp.25.4.363

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


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  8 in total

1.  Metachromatic leucoencephalopathy: a form of lipidosis.

Authors:  R M NORMAN; H URICH; A H TINGEY
Journal:  Brain       Date:  1960-09       Impact factor: 13.501

2.  Cerebellar hypoplasia in Werdnig-Hoffmann disease.

Authors:  R M NORMAN
Journal:  Arch Dis Child       Date:  1961-02       Impact factor: 3.791

3.  Histological and chemical findings in Krabbe's leucodystrophy.

Authors:  R M NORMAN; D R OPPENHEIMER; A H TINGEY
Journal:  J Neurol Neurosurg Psychiatry       Date:  1961-08       Impact factor: 10.154

4.  Leukodystrophy and the concept of dysmyelination.

Authors:  C M POSER
Journal:  Arch Neurol       Date:  1961-03

5.  [On non-metachromatic leukodystrophy].

Authors:  J PEIFFER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1959

6.  Dysgenetic gliosis of the brain; a case of macrogyria.

Authors:  W KRAMER
Journal:  J Neuropathol Exp Neurol       Date:  1956-10       Impact factor: 3.685

7.  Natural history and evolution of the concept of Schilder's diffuse sclerosis.

Authors:  C M POSER; L VAN BOGAERT
Journal:  Acta Psychiatr Neurol Scand       Date:  1956

8.  [Merzbacher-Pelizaeus disease; clinico-anatomic studies of its position among the diffuse scleroses].

Authors:  F SEITELBERGER
Journal:  Wien Z Nervenheilkd Grenzgeb       Date:  1954
  8 in total
  9 in total

1.  [ON THE DEGREE OF VARIATION IN PELIZAEUS-MERZBACHER DISEASE. (WITH A CONTRIBUTION TO FAMILIAL MULTIPLE SCLEROSIS)].

Authors:  J PEIFFER; E ZERBIN-RUEDIN
Journal:  Acta Neuropathol       Date:  1963-11-05       Impact factor: 17.088

2.  Cerebral malformation associated with metabolic disorder. A report of 2 cases.

Authors:  M Erdohazi; N D Barnes; M J Robinson; B D Lake
Journal:  Acta Neuropathol       Date:  1976-12-21       Impact factor: 17.088

3.  Pelizaeus-Merzbacher disease in a brother and sister.

Authors:  R Pamphlett; P Silberstein
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

4.  Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease.

Authors:  J J Martin; R Deberdt; M Philippart; K J Van Acker; C Hooft
Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

5.  [Genetic contribution to the problem of the late form of Pelizaeus-Merzbacher disease].

Authors:  E Zerbin-Rüdin; J Peiffer
Journal:  Humangenetik       Date:  1964

6.  Lissencephaly and Pachygyria: an architectonic and topographical analysis.

Authors:  R M Stewart; D P Richman; V S Caviness
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

7.  The value of CT in diagnosis and prognosis of different inborn neurodegenerative disorders in childhood.

Authors:  S Wende; B Ludwig; T Kishikawa; M Rochel; J Gehler
Journal:  J Neurol       Date:  1984       Impact factor: 4.849

8.  Computed tomography in Pelizaeus-Merzbacher disease.

Authors:  A Statz; E Boltshauser; A Schinzel; H Spiess
Journal:  Neuroradiology       Date:  1981       Impact factor: 2.804

9.  Intrauterine multisystem atrophy in siblings: a new genetic syndrome?

Authors:  M K Herrick; A M Strefling; H Urich
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

  9 in total

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