(Q39928081)

15 September 2017

1 reference

title

Epidemiology of Motor-Neuron Diseases (English)

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

7 February 2023

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4576955

7 February 2023

author name string

Bobowick AR

1

1 reference

15 September 2017

Brody JA

2

1 reference

15 September 2017

language of work or name

English

0 references

publication date

1 May 1973

1 reference

15 September 2017

17 May 1973

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4576955

full work available at URL

7 February 2023

http://www.nejm.org/doi/pdf/10.1056/NEJM197305172882005

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The New England Journal of Medicine

7 February 2023

published in

1 reference

15 September 2017

288

1 reference

15 September 2017

20

1 reference

15 September 2017

1047-1055

1 reference

"Myopathic" Changes in Chronically Denervated Muscle

15 September 2017

1

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases

7 February 2023

2

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease

7 February 2023

3

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

"Sick" motoneurones. A unifying concept of muscle disease

7 February 2023

4

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

7 February 2023

5

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

7 February 2023

6

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Incidence of selected congenital malformations in Iowa

7 February 2023

8

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Hereditary non-progressive muscular dystrophy inducing arthrogryposis syndrome.

7 February 2023

9

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence.

7 February 2023

10

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

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

7 February 2023

11

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Lower motor neuron deficit in arthrogryposis. An EMG study

7 February 2023

12

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Helvetica paediatrica acta

7 February 2023

13

15

259

Frischknecht

1960

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Hereditary factors in infantile progressive muscular atrophy; study of 112 cases in 70 families

7 February 2023

16

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Course and symptoms of progressive infantile muscular atrophy; a follow-up study of 112 cases in Denmark.

7 February 2023

17

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

HISTOCHEMISTRY OF MUSCLE IN INFANTILE SPINAL MUSCULAR ATROPHY

7 February 2023

20

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

7 February 2023

22

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Chronic proximal spinal muscular atrophy

7 February 2023

23

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

THE WOHLFART-KUGELBERG-WELANDER DISEASE; REVIEW OF THE LITERATURE AND REPORT OF A CASE.

7 February 2023

24

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Kugelberg-Welander disease with particular reference to sex-influenced manifestations

7 February 2023

25

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Neurogenic Muscular Atrophy Simulating Muscular Dystrophy

7 February 2023

26

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Kugelberg-Welander Syndrome (Hereditary Proximal Spinal Muscular Atrophy)

7 February 2023

27

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Kugelberg-welander syndrome with dominant inheritance

7 February 2023

28

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Familial Proximal Spinal Muscular Atrophy

7 February 2023

29

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

A new genetic variant of spinal muscular atrophy

7 February 2023

30

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Chronic spinal muscular atrophy in adults. 1. The Kugelberg-Welander syndrome

7 February 2023

31

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The Ryukyuan muscular atrophy. An obscure heritable neuromuscular disease found in the islands of southern Japan

7 February 2023

32

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Progressive bulbar paralysis in childhood (Fazio-Londe's disease). Report of a case with pathologic evidence of nuclear atrophy

7 February 2023

33

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Familial progressive bulbar‐spinal muscular atrophy

7 February 2023

34

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

HEREDITARY PROXIMAL NEUROGENIC MUSCULAR ATROPHY IN ADULT

7 February 2023

35

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Proximal spinal muscular atrophy

7 February 2023

36

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The benign proximal spinal progressive muscular atrophies

7 February 2023

37

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

7 February 2023

38

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance: Kugelberg-Welander disease and its variant of late onset in one pedigree

7 February 2023

39

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Chronic spinal muscular atrophy in adults. 2. Other forms

7 February 2023

41

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Deutsche Zeitschrift fur Nervenheilkunde

7 February 2023

42

188

1

Hallen

1966

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form

7 February 2023

43

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy With particular reference to the heterogeneity of Kugelberg-Welander disease

7 February 2023

44

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Journal de genetique humaine

7 February 2023

45

7

1

Stark

1958

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Scapuloperoneal muscular atrophy

7 February 2023

46

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The Neurogenic Scapulo-Peroneal Syndrome

7 February 2023

47

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Bulletin of the Los Angeles neurological societies

7 February 2023

48

35

47

Feigenbaum

1970

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Distal type of chronic spinal muscular atrophy. Clinical, electrophysiological and pathological studies

7 February 2023

50

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

A distal form of chronic spinal muscular atrophy

7 February 2023

51

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.

7 February 2023

52

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

FAMILIAL MOTOR NEURONE DISEASE.

7 February 2023

53

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Hereditary amyotrophic lateral sclerosis

7 February 2023

54

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

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

7 February 2023

55

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

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

7 February 2023

56

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Amyotrophic lateral sclerosis

7 February 2023

61

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Proceedings of the staff meetings. Mayo Clinic

7 February 2023

62

32

427

Mulder

1957

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

7 February 2023

65

78

827

Bonduelle

1970

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Prognosis of amyotrophic lateral sclerosis

7 February 2023

66

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The reliability of death certificate reporting for amyotrophic lateral sclerosis

7 February 2023

68

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Epidemiologic study of amyotrophic lateral sclerosis in Hawaii. Identification of high incidence among Filipino men.

7 February 2023

70

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Mexican "Resistance" to Amyotrophic Lateral Sclerosis

7 February 2023

71

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Amyotrophic lateral sclerosis mortality among native-born and migrant residents of California and Washington

7 February 2023

72

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Multiple sclerosis among American, Japanese and Chinese migrants to California and Washington

7 February 2023

73

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Descriptive epidemiology of selected neurologic and myopathic disorders with particular reference to a survey in Rochester, Minnesota

7 February 2023

74

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Acta Neurologica Scandinavica

7 February 2023

75

42

8

Brewis

1966

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The prevalence of some neurological diseases in Iceland

7 February 2023

76

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Schweizerische medizinische Wochenschrift

7 February 2023

78

99

51

Lorez

1969

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Studii si cercetari de neurologie

7 February 2023

79

9

401

Kreindler

1964

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Multiple sclerosis and amyotrophic lateral sclerosis in Mississippi

7 February 2023

83

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Amyotrophic Lateral Sclerosis and Metallic Toxins

7 February 2023

84

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

7 February 2023

La Medicina del lavoro

85

59

721

Capellini

1968

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

A syndrome clinically resembling amyotrophic lateral sclerosis following chronic mercurialism

7 February 2023

86

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Depressed Monoamine Catabolite Levels in Cerebrospinal Fluid of Patients with Parkinsonism Dementia of Guam

7 February 2023

87

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

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

7 February 2023

88

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Amyotrophic lateral sclerosis. A study of central monoamine metabolism and therapeutic trial of levodopa

7 February 2023

89

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

A cutaneous disorder of connective tissue in amyotrophic lateral sclerosis. A histochemical study

7 February 2023

90

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Collagenolytic activity of the skin associated with neuromuscular diseases including amyotrophic lateral sclerosis

7 February 2023

91

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Vascular and metabolic studies of amyotrophic lateral sclerosis. I. Angiopathy in biopsy specimens of peripheral arteries

7 February 2023

92

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Vascular and metabolic studies of amyotrophic lateral sclerosis. I. Angiopathy in biopsy specimens of peripheral arteries

7 February 2023

93

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Motor neurone disease. Further evidence for an abnormality of nerve metabolism

7 February 2023

94

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Psychological function in individuals with amyotrophic lateral sclerosis (ALS)

7 February 2023

95

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Epidemiologic Features of Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia in Guam, Mariana Islands

7 February 2023

97

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Patterns of Neurologic Diseases on Guam

7 February 2023

98

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

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

7 February 2023

99

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Proceedings of the Australian Association of Neurologists

7 February 2023

101

5

335

Yase

1968

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Epidemiological study of amyotrophic lateral sclerosis and allied disorders in the Kii peninsula (Japan)

7 February 2023

103

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Motor-neuron disease in natives of New Guinea

7 February 2023

104

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

NEUROLOGICAL DISORDERS IN THE ZULU.

7 February 2023

106

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

The pattern of neurological illness in tropical Africa. Experience at Ibadan, Nigeria

7 February 2023

107

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

Patterns of neurological practice in Calcutta and West Bengal (India).

7 February 2023

108

1 reference

https://api.crossref.org/works/10.1056/NEJM197305172882005

7 February 2023

Identifiers

1 reference

15 September 2017

1 reference