(Q33586630)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

22 May 2022

author name string

P. K. Thomas

series ordinal

1

1 reference

full work available at URL

22 May 2022

language of work or name

English

0 references

publication date

1 December 1975

1 reference

28 July 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/176361/pdf/?tool=EBI

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/176361/?tool=EBI

22 May 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

http://jmg.bmjjournals.com/cgi/content/abstract/12/4/317

22 May 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

https://europepmc.org/articles/PMC1013309

22 May 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

https://europepmc.org/articles/PMC1013309?pdf=render

22 May 2022

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A176361

https://syndication.highwire.org/content/doi/10.1136/jmg.12.4.317

22 May 2022

1 reference

https://api.crossref.org/works/10.1136/JMG.12.4.317

Journal of Medical Genetics

22 May 2022

published in

1 reference

28 July 2017

12

1 reference

28 July 2017

317-326

1 reference

28 July 2017

4

1 reference

28 July 2017

Hereditary sensory radicular neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

CYTOGENETIC STUDIES IN FAMILIAL MEDITERRANEAN FEVER.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

NINE CASES OF HEREDITARY AND NON-HEREDITARY PERIODIC DISEASES.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

THE INHERITED AMYLOIDOSES: THEIR CLINICAL AND THEORETICAL SIGNIFICANCE

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

A study of the fine structure of the amyloid associated with familial Mediterranean fever

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Amyloidosis as the sole manifestation of familial Mediterranean fever (FMF). Further evidence of its genetic nature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Inheritance of primary systemic amyloidosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Amyloidosis in familial Mediterranean fever. An independent genetically determined character

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Siegel-Cattan-Mamou's disease; paroxysmal abacterial peritonitis with pleuropericardial and articular complications; autonomous clinical form of Reiman's periodic disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Primary systemic amyloidosis: a review and an experimental, genetic, and clinical study of 29 cases with particular emphasis on the familial form

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Periodic peritonitis; heredity and pathology: report of seventy-two cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial Mediterranean fever among the Turkish people

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial Mediterranean Fever in an Italian Family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial Mediterranean fever. A survey of 470 cases and review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

The genetic amyloidoses with particular reference to hereditary neuropathic amyloidosis, type II (Indiana or Rukavina type)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Hereditary cerebral haemorrhage with amyloidosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Peripheral nerve changes in amyloid neuropathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial amyloid polyneuropathy: an electron microscope study of the peripheral nerve in five cases. II. Nerve fibre changes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial amyloid polyneuropathy: an electron microscope study of the peripheral nerve in five cases. I. Interstitial changes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Giant cell arteritis and arteriolitis associated with amyloid angiopathy in an elderly mongol.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Relationship of amyloid to aging. Review of the literature and systematic study of 83 patients derived rom a general hospital population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Vascular changes in Alzheimer's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Peripheral neuropathy in familial primary amyloidosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Amyloidosis cutis. Familial occurrence in three generations

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

An unusual type of pre-senile dementia (atypical Alzheimer's disease with amyloid vascular change).

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Familial perireticular amyloidosis in a Swedish family

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Polyneuritic amyloidosis in a Japanese family

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013309

Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2

31 October 2018

1 reference

12 December 2020

Renal biopsy findings in familial amyloidosis with corneal lattice dystrophy. An immuno-histochemical, light-microscopical and electron-microscopical study

1 reference

12 December 2020

Primary Neuropathic Amyloidosis in Three Brothers

1 reference

12 December 2020

Amyloidotic Polyneuritis of Type III (Iowa-Van Allen)

1 reference

12 December 2020

Portuguese type of familial amyloid polyneuropathy. Anatomo-clinical study of a Brazilian family

1 reference

12 December 2020

AMYLOIDOSIS: ITS DIFFERENTIATION INTO PERIRETICULIN AND PERI-COLLAGEN TYPES

1 reference

12 December 2020

A CASE OF PERIPHERAL NEUROPATHY IN FAMILIAL PRIMARY AMYLOIDOSIS

1 reference

12 December 2020

PORTUGUESE POLYNEURITIC FAMILIAL TYPE OF AMYLOIDOSIS

1 reference

12 December 2020

CLASSIFICATION OF AMYLOIDOSIS WITH SPECIAL REGARD TO THE GENETIC TYPES

1 reference

12 December 2020

Amylogenic periodic disease

1 reference

12 December 2020

[Primary amyloidosis with meningo-radiculo-neuritic complication]

1 reference

12 December 2020

Vitreous Opacities Diagnostic of Familial Primary Amyloidosis

1 reference

12 December 2020

Persistent atrial standstill in a family with myocardial disease

1 reference

12 December 2020

Hereditary amyloidosis, the flexor retinaculum, and the carpal tunnel syndrome

1 reference

12 December 2020

Hereditary amyloidosis with polyneuropathy

1 reference

12 December 2020

Hereditary amyloidosis

1 reference

12 December 2020

Familial Occurrence of Parathyroid Adenomas, Pheochromocytoma, and Medullary Carcinoma of the Thyroid with Amyloid Stroma (Sipple's Syndrome)

1 reference

12 December 2020

Amyloidosis, Deafness, Urticaria, and Limb Pains: A Hereditary Syndrome

1 reference

12 December 2020

The genetic aspect of the familial amyloidotic polyneuropathy. Portuguese type of paramyloidosis

1 reference

12 December 2020

Dissociated sensation in amylidosis. Compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies

1 reference

12 December 2020

Familial primary amyloidosis

1 reference

12 December 2020

Familial amyloid-producing medullary thyroid carcinoma and pheochromocytoma. A distinct genetic entity

1 reference

12 December 2020

Chromosome studies in familial pericollagenous amyloidosis

1 reference

12 December 2020

Familial amyloid polyneuropathy, type Wohlwill-Corino Andrade

1 reference

12 December 2020

Amyloidosis presenting as urticaria

1 reference

12 December 2020

Primary familial amyloidosis. Ocular manifestations with histopathologic observations

1 reference

12 December 2020

Familial primary amyloidosis with nervous system involvement

1 reference

12 December 2020

[Optical polarization studies of amyloid substance]

1 reference

12 December 2020

Ocular manifestations of hereditary primary systemic amyloidosis

1 reference

12 December 2020

[Pathological anatomy of Portuguese cases of paramyeloidosis with special reference to the peripheral nervous system]

1 reference

12 December 2020

[The periodic disease; 38 personal cases]

1 reference

12 December 2020

Familial primary systemic amyloidosis: an experimental, genetic and clinical study

1 reference

12 December 2020

Familial Mediterranean fever

1 reference

12 December 2020

Primary familial amyloidosis

1 reference

12 December 2020

Cardiac involvement in a peculiar form of paramyloidosis

1 reference

12 December 2020

Familial endocrine tumors; report of two unrelated kindred affected with pheochromocytomas, one also with multiple thyroid carcinomas

1 reference

12 December 2020

Familial primary amyloidosis with severe amyloid heart disease

1 reference

12 December 2020

[PARAMYLOIDOSIS OF PERIPHERAL NERVES IN PORTUGAL]

1 reference

12 December 2020

Clinical manifestations and diagnosis of amyloid polyneuropathy. Report of three cases

1 reference

12 December 2020

[The periodic disease]

1 reference

12 December 2020

Localized amyloidosis cutis associated with psoriasis in siblings

1 reference

12 December 2020

Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation. Report on three cases

1 reference

12 December 2020

Amyloid in corneal dystrophies. Differentiation of lattice from granular and macular dystrophies

1 reference

12 December 2020

Creatinine-clearnace nomogram

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.12.4.317

1 reference

National Center for Biotechnology Information

PubMed ID

176361