Endocrine dysfunction in patients with Fabry disease.

Endocrine dysfunction in patients with Fabry disease.

Item
http://www.wikidata.org/entity/Q43776388
A mouse model suggests two mechanisms for thyroid alterations in infantile cystinosis: decreased thyroglobulin synthesis due to endoplasmic reticulum stress/unfolded protein response and impaired lysosomal processing.Quality of life in patients with Fabry disease: a systematic review of the literature.Endocrine manifestations related to inherited metabolic diseases in adults.Fabry disease superimposed on overt autoimmune hypothyroidismHypothyroidism in late-onset Pompe disease.Perspectives in Pediatric Pathology, Chapter 21. Testicular Pathology in Heritable Metabolic Disease.Switch to agalsidase alfa after shortage of agalsidase beta in Fabry disease: a systematic review and meta-analysis of the literature.Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases.Pituitary function and morphology in Fabry disease.Fabry disease
P2860

Endocrine dysfunction in patients with Fabry disease.

Item
http://www.wikidata.org/entity/Q43776388
description
2006 nî lūn-bûn
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2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
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2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
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2006年学术文章
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2006年學術文章
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2006年學術文章
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name
Endocrine dysfunction in patients with Fabry disease.
@en
Endocrine dysfunction in patients with Fabry disease.
@nl
type
label
Endocrine dysfunction in patients with Fabry disease.
@en
Endocrine dysfunction in patients with Fabry disease.
@nl
prefLabel
Endocrine dysfunction in patients with Fabry disease.
@en
Endocrine dysfunction in patients with Fabry disease.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Endocrine dysfunction in patients with Fabry disease
@en
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698