(Q69786791)

English

Persistent skin ulcers, mutilations, and acro-osteolysis in hereditary sensory and autonomic neuropathy with phospholipid excretion. Report of a family

scientific article published on 01 October 1989

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

Persistent skin ulcers, mutilations, and acro-osteolysis in hereditary sensory and autonomic neuropathy with phospholipid excretion. Report of a family (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

hereditary sensory and autonomic neuropathy

0 references

1 reference

based on heuristic

inferred from title

autonomic neuropathy

1 reference

based on heuristic

inferred from title

author name string

M Böckers

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

P Benes

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

K Bork

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

language of work or name

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publication date

1 October 1989

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

Journal of the American Academy of Dermatology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

21

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

4 Pt 1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

736-739

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary sensory neuropathy with neurotrophic keratitis. Description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathies

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Plantar ulcers in hereditary sensory neuropathy. A plea for conservative treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

[Ulceromutilating acroosteopathy of the feet (author's transl)]

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The clinical spectrum and morphology of type II hereditary sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary sensory neuropathy, type II. Clinical, electrophysiologic, histologic, and biochemical studies of a Quebec kinship.

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

PROGRESSIVE SENSORY NEUROPATHY IN CHILDREN

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Lipid abnormalities in hereditary neuropathy. Part 3. Plasma and erythrocyte lipids of HMSN-III (Dejerine-Sottas disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Lipid abnormalities in hereditary neuropathy. Part 4. Endoneurial and liver lipids of HMSN-III (Déjerine-Sottas disease)

1 reference

https://api.crossref.org/works/10.1016%2FS0190-9622%2889%2970247-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0190-9622(89)70247-4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2808789%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

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