(Q70005908)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

title

[Recessive hereditary amyotrophic lateral sclerosis with "Lafora bodies" (author's transl)] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

7 October 2019

main subject

1 reference

H Orthner

1

1 reference

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7 October 2019

P E Becker

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

D Müller

series ordinal

3

1 reference

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7 October 2019

publication date

1 October 1973

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

volume

217

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

issue

4

1 reference

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7 October 2019

page(s)

387-412

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

Lafora's disease in the dog. A comparative study

7 October 2019

cites work

1 reference

12 December 2020

TWO CASES OF ATYPICAL SPINAL PROGRESSIVE MUSCULAR ATROPHY (LUMBOSACRAL LEG-THIGH TYPE). A CLINICOPATHOLOGICAL STUDY WITH THE SURVEY OF THE RELEVANT LITERATURE

1 reference

12 December 2020

[Myoclonic bodies and progressive myoclonic epilepsy]

1 reference

12 December 2020

[Duration of disease and prognosis of different types of myatrophic lateral sclerosis and spinal muscular atrophy; catamnestic examinations]

1 reference

12 December 2020

[Familial amyotrophic lateral sclerosis. Clinical study]

1 reference

12 December 2020

The central nervous system in motor neurone disease

1 reference

12 December 2020

[The myatrophic lateral sclerosis. Clinical, electromyographic and biopsy-histological studies on 112 patients]

1 reference

12 December 2020

A case of Pick's disease with terminal amyotrophic lateral sclerosis. Contribution to the temporal semiology

1 reference

12 December 2020

Amyotrophic lateral sclerosis. Association with schizophrenic symptoms and showing Alzheimer's tangles

1 reference

12 December 2020

Amyotrophic lateral sclerosis-dementia complex, neuroaxonal dystrophy, and Hallervorden-Spatz disease

1 reference

12 December 2020

Ultrastructure of Hirano bodies.

1 reference

12 December 2020

Central nervous system deposits in protractive (Lundborg-type myoclonic bodies disease

1 reference

12 December 2020

An inherited disease similar to amyotrophic lateral sclerosis with a pattern of posterior column involvement. An intermediate form?

1 reference

12 December 2020

A study of rod-like structures (Hirano bodies) in 240 normal and pathological brains.

1 reference

12 December 2020

Amyotrophic lateral sclerosis with progressive dementia and with pathologic findigs of the Creutzfeldt-Jakob syndrome.

1 reference

12 December 2020

Studies in myoclonus epilepsy (Lafora body form). I. Isolation and preliminary characterization of Lafora bodies in two cases.

1 reference

12 December 2020

Correlation between ultrastructure and histochemistry of lafora bodies

1 reference

12 December 2020

FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS WITH PSEUDO-MYOPATHIC ONSET

1 reference

12 December 2020

Myoclonic epilepsy with lafora bodies. Some ultrastructural, histochemical, and biochemical aspects.

1 reference

12 December 2020

[Different forms of myatrophic lateral sclerosis]

1 reference

12 December 2020

Intraneuronal conglomerates in sporadic motor neuron disease. A light and electron microscopic study.

1 reference

12 December 2020

Presenile dementia with "Lafora-like" intraneuronal inclusions

1 reference

12 December 2020

A histochemical study on myoclonus-epilepsy (Lafora-body type).

1 reference

12 December 2020

Amyotrophic lateral sclerosis. Clinicopathological studies of a family

1 reference

12 December 2020

Amyotrophic lateral sclerosis. A comparison of Guam and classical cases.

1 reference

12 December 2020

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

1 reference

12 December 2020

FAMILIAL MOTOR NEURONE DISEASE.

1 reference

12 December 2020

Familial occurrence of a bulbar paralytic form of amyotropic lateral sclerosis with reticular corneal dystrophy and cutis hyperelastica in 3 sisters

1 reference

12 December 2020

Studies in myoclonus epilepsy (Lafora body form). II. Polyglucosans in the systemic deposits of myoclonus epilepsy and in corpora amylacea

1 reference

12 December 2020

Subacute degeneration of peripheral motor neurons with neuron inclusions and posterior column lesions: extent of amyotrophic lateral sclerosis

1 reference

12 December 2020

Sporadic juvenile amyotrophic lateral sclerosis. A clinicopathological study of a case with neuronal cytoplasmic inclusions containing RNA.

1 reference

12 December 2020

The fine structure of some intraganglionic alterations. Neurofibrillary tangles, granulovacuolar bodies and "rod-like" structures as seen in Guam amyotrophic lateral sclerosis and parkinsonism-dementia complex

1 reference

12 December 2020

Amyotrophic Lateral Sclerosis and degenerative lesions of the posterior column

1 reference

12 December 2020

Parkinsonism-dementia complex, an endemic disease on the island of Guam. II. Pathological features

1 reference

12 December 2020

Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons

1 reference

12 December 2020

STUDY OF THE ETIOLOGY OF AMYOTROPHIC LATERAL SCLEROSIS

1 reference

12 December 2020

[C2 cases of torsion spasm accompanied by chorioathetosis with numerous Lafora bodies in the external part of the globus pallidus].

1 reference

12 December 2020

[Histochemical studies on myoclonus bodies in progressive myoclonus epilepsy (Unverricht type)]

1 reference

12 December 2020

Proximal axonal enlargement in motor neuron disease.

1 reference

12 December 2020

[THE MYOCLONUS BODY DISEASE. A CONGENITAL DISORDER OF THE CARBOHYDRATE METABOLISM. CLINICOPATHOLOGICAL STUDY OF 5 CASES.]

1 reference

12 December 2020

General neuropathology of degenerative processes of the nervous system

1 reference

12 December 2020

Ultrastructure of Lafora bodies

1 reference

12 December 2020

Ninhydrin-Schiff and alloxan-Schiff staining; a new histochemical staining method for protein

1 reference

12 December 2020

[On the substructure of myoclonus bodies in progressive myoclonus epilepsy (Unverricht-type)]

1 reference

12 December 2020

Hereditary amyotrophic lateral sclerosis

1 reference

12 December 2020

Juvenile amyotrophic lateral sclerosis-dementia complex in a Dutch family

1 reference

12 December 2020

[On the ultrastructure of myoclonic bodies]

1 reference

12 December 2020

[Histochemical study of Lafora's bodies]

1 reference

12 December 2020

Discussion of the report on progressive myoclonic epilepsy

1 reference

12 December 2020

[Hereditary cerebellar aataxia with spinal muscular atrophies]

1 reference

12 December 2020

A METHOD FOR THE CYTOPHOTOMETRIC ESTIMATION OF NUCLEIC ACIDS USING METHYLENE BLUE.

1 reference

12 December 2020

Myoclonus epilepsy with Lafora bodies: case report with electron microscopic observation.

1 reference

12 December 2020

Microphotometric analysis of the cytochemical Millon reaction

1 reference

12 December 2020

Histophysical and histochemical investigations of myoclonus bodies.

1 reference

12 December 2020

Amyotrophic lateral sclerosis and Parkinsonism-dementia complex on Guam. Further pathologic studies

1 reference

12 December 2020

Parkinsonism-dementia complex, an endemic disease on the island of Guam. I. Clinical features.

1 reference

12 December 2020

Familial motor neuron disease, non-Chamorro type: report of kinship

1 reference

12 December 2020

Recent neuropathologic observations in amyotrophic lateral sclerosis and parkinsonism‐dementia of Guam

1 reference

12 December 2020

Amyotrophic lateral sclerosis and parkinsonism dementia in a migrant population from Guam.

1 reference

12 December 2020

Combination of amyotrophic lateral sclerosis with Pick's disease

1 reference

12 December 2020

Ultrastructure of anterior horn motor neurones in the Hirano-Kurland-Sayre type of combined neurological system degeneration

1 reference

12 December 2020

Neurofibrillary pathology.

1 reference

12 December 2020

Parkinsonism-dementia and amyotrophic lateral sclerosis of Guam. Effect of probenecid on monoamine catabolite levels in cerebrospinal fluid.

1 reference

12 December 2020

Progressive familial myoclonic epilepsy with Lafora bodies. Electron microscopic and histochemical study of a cerebral biopsy.

1 reference

12 December 2020

A study of the late form (type Lundborg) of progressive myoclonic epilepsy.

1 reference

12 December 2020

FAMILIAL AMYOTROPHIC LATEAL SCLEROSIS. (CLINICAL CONTRIBUTION)

1 reference

12 December 2020

[Simultaneous development of amyotrophic lateral sclerosis, Parkinson's syndrome and progressive dementia. Apropos of 2 anatomoclinical cases. Attempted interpretation]

1 reference

12 December 2020

[Typical amyotrophic lateral sclerosis and hereditary paralysis agitans in the same family with the possibility of a form transitional between the two]

1 reference

12 December 2020

[Duration of various forms of amyotrophic lateral sclerosis]

1 reference

12 December 2020

Cytophotometric studies on the staining dichroism of Lafora bodies (Lafora bodies)

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02552701

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4129370%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

1 reference