The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
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Lymph vessels: the forgotten second circulation in health and diseaseThe lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature reviewEPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.Lymph flow regulates collecting lymphatic vessel maturation in vivo.A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like diseaseGenetics of lymphatic anomaliesNovel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.Congenital generalized lymphangiectasia: a rare developmental disorder for non-immune fetal hydropsFoxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivationPrimary Intestinal Lymphangiectasia Manifested as Unusual Edemas and Effusions: A Case ReportNew developments in clinical aspects of lymphatic disease.Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.A tale of two models: mouse and zebrafish as complementary models for lymphatic studies.Childhood lymphoedema and 'Lymphaletics': overcoming barriers.VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations.Human diseases associated with connexin mutations.Managing ulceration and lymphorrhea in chronic oedema.Vascular heterogeneity and specialization in development and disease.A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis.Aetiology, comorbidities and cofactors of chronic leg ulcers: retrospective evaluation of 1 000 patients from 10 specialised dermatological wound care centers in Germany.Health-related quality of life in patients with lymphoedema - a cross-sectional study.Systematic review of lymphovenous anastomosis (LVA) for the treatment of lymphedema.Audit of skin changes present in referrals to a specialist lymphoedema service.Circumferential suction-assisted lipectomy in the treatment of primary and secondary end-stage lymphoedema of the leg.Lymphoedema of the upper limb: a rare complication of thyroid surgery?Specialized consultations in a hospital-based referral center for patients suspected of having limb lymphedema: Impact on diagnosis.A Novel Splice-Site Mutation in Is Associated with Congenital Primary Lymphoedema of Gordon
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P2860
The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
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name
The classification and diagnos ...... to include molecular findings.
@en
type
label
The classification and diagnos ...... to include molecular findings.
@en
prefLabel
The classification and diagnos ...... to include molecular findings.
@en
P2093
P2860
P356
P1433
P1476
The classification and diagnos ...... to include molecular findings
@en
P2093
P2860
P304
P356
10.1111/CGE.12173
P577
2013-06-27T00:00:00Z