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Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema

Physiological reviews, 2021-10, Vol.101 (4), p.1809-1871

2021

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Self-care treatment for lymphoedema of lymphatic filariasis using integrative medicine

British journal of dermatology (1951), 2023-12, Vol.190 (1), p.94-104

2023

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Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort

PloS one, 2022-10, Vol.17 (10), p.e0274867-e0274867

2022

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EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis

The Journal of clinical investigation, 2016-08, Vol.126 (8), p.3080-3088

2016

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Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

American journal of human genetics, 2012-02, Vol.90 (2), p.356-362

2012

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Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition

Frontiers in genetics, 2022-09, Vol.13, p.1001105

2022

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PSENEN and NCSTN Mutations in Familial Hidradenitis Suppurativa (Acne Inversa)

Journal of investigative dermatology, 2011-07, Vol.131 (7), p.1568-1570

2011

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New developments in clinical aspects of lymphatic disease

The Journal of clinical investigation, 2014-03, Vol.124 (3), p.915-921

2014

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A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon

International journal of molecular sciences, 2018-08, Vol.19 (8), p.2259

2018

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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

Nature communications, 2019-04, Vol.10 (1), p.1951-1951, Article 1951

2019

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Recent advances in breast cancer-related lymphedema of the arm: lymphatic pump failure and predisposing factors

Lymphatic research and biology, 2009-03, Vol.7 (1), p.29

2009

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Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

JCI insight, 2023-10, Vol.8 (20)

2023

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Popliteal node visualization during standard pedal lymphoscintigraphy for a swollen limb indicates impaired lymph drainage

American journal of roentgenology (1976), 2011-12, Vol.197 (6), p.1443

2011

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Lymphatic drainage in the muscle and subcutis of the arm after breast cancer treatment

Breast cancer research and treatment, 2009-10, Vol.117 (3), p.549-557

2009

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Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

Nature communications, 2015-09, Vol.6 (1), p.8085-8085, Article 8085

2015

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A Genetic Approach to the Classification of Primary Lymphoedema and Lymphatic Malformations

European journal of vascular and endovascular surgery, 2018-10, Vol.56 (4), p.465-466

2018

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Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

Nature genetics, 2011-10, Vol.43 (10), p.929-931

2011

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Phase II study of ceralasertib (AZD6738) in combination with durvalumab in patients with advanced gastric cancer

Journal for immunotherapy of cancer, 2022-07, Vol.10 (7), p.e005041

2022

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Systematic Review of Magnetic Resonance Lymphangiography From a Technical Perspective

Journal of magnetic resonance imaging, 2021-06, Vol.53 (6), p.1766-1790

2021

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Assessment of health-related quality of life in patients with lymphedema of the lower limb

Wound repair and regeneration, 2006-03, Vol.14 (2), p.110-118

2006

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Mutations in the γ-Secretase Genes NCSTN, PSENEN, and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa)

Journal of investigative dermatology, 2012-10, Vol.132 (10), p.2459-2461

2012

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Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema

Circulation research, 2013-03, Vol.112 (6), p.956-960

2013

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Structural Skin Capillary Rarefaction in Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1999-04, Vol.33 (4), p.998-1001

1999

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Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency

Journal of vascular research, 2011-01, Vol.48 (5), p.397-407

2011

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Lipedema: An inherited condition

American journal of medical genetics. Part A, 2010-04, Vol.152A (4), p.970-976

2010

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Development and physiological functions of the lymphatic system: insights from human genetic studies of primary lymphedema

Self-care treatment for lymphoedema of lymphatic filariasis using integrative medicine

Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort

EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis

Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition

PSENEN and NCSTN Mutations in Familial Hidradenitis Suppurativa (Acne Inversa)

New developments in clinical aspects of lymphatic disease

A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

Recent advances in breast cancer-related lymphedema of the arm: lymphatic pump failure and predisposing factors

Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies

Popliteal node visualization during standard pedal lymphoscintigraphy for a swollen limb indicates impaired lymph drainage

Lymphatic drainage in the muscle and subcutis of the arm after breast cancer treatment

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

A Genetic Approach to the Classification of Primary Lymphoedema and Lymphatic Malformations

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

Phase II study of ceralasertib (AZD6738) in combination with durvalumab in patients with advanced gastric cancer

Systematic Review of Magnetic Resonance Lymphangiography From a Technical Perspective

Assessment of health-related quality of life in patients with lymphedema of the lower limb

Mutations in the γ-Secretase Genes NCSTN, PSENEN, and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa)

Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema

Structural Skin Capillary Rarefaction in Essential Hypertension

Mutations in FOXC2 in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency

Lipedema: An inherited condition

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