about
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.Magnetic Resonance Imaging-Based Assessment of Breast Cancer-Related Lymphoedema Tissue Composition.Quantitative Contrast-Enhanced Magnetic Resonance Lymphangiography of the Upper Limbs in Breast Cancer Related Lymphedema: An Exploratory Study.Surgical procedures in lymphedema management.Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations.Ano-genital Granulomatosis and Crohn's Disease: A Case Series of Males Presenting with Genital Lymphoedema.A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy.An unusual case of genital swellingA Novel Splice-Site Mutation in Is Associated with Congenital Primary Lymphoedema of GordonLipedema: An inherited conditionMosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapyProgressive lymphangiomatosis and Gorham's disease: case report and clinical implicationsPhotoaggravated Sweet's syndromeRapid resolution of hidradenitis suppurativa after bariatric surgical interventionA Genetic Approach to the Classification of Primary Lymphoedema and Lymphatic MalformationsPostzygotic mosaicism in a woman with Goltz syndrome mimics segmental angioma serpiginosum
P50
Q26750211-8418CF7A-C2E8-491D-92C9-853393354188Q26825187-0BB0EDF9-E7DA-412E-AA22-192A1A0E5566Q27329626-8CA556CF-8BFF-4701-91A5-E9683A8AE104Q30491756-AC244F10-B0AE-49BF-9D39-27535F5EAFF9Q35821814-19F13CCD-C937-421E-BC31-BFA6E528ACD3Q35963398-8AA68184-9F83-435B-8967-E9F854D6AAE5Q36055794-3A0910F5-095D-443D-86D1-A45EF850708FQ37058507-6EBA2DB8-4ADE-4B59-985C-BE12206A46E0Q37609931-76C580FF-4367-4033-AD10-F56830921ADEQ38052872-C47DD8AD-C0A7-45C6-ABED-7645718D855EQ38102064-AC298EFB-C5F4-4E82-AFEE-7F963B5E580AQ38621448-6214D811-3D65-4144-B45B-93F0905D7D09Q38967588-07A6672A-EE80-46DC-99AB-E024425A1FFEQ46087914-C46619F2-9FC1-4C71-AB1D-E8895B8A5735Q50422507-15EF8304-14FC-4225-B452-606E71DD94FDQ56112368-E3FEC593-A24F-4123-B6E1-29E871BDA183Q57150749-08998A57-7656-4614-A45A-084130636432Q57150860-14B42FC3-7511-47FF-9114-B18B80A78604Q58081557-6CB157EA-B44E-44F4-BF76-13C23764F4FCQ83129337-1603CA46-61FB-4A6A-BF15-4ADE7C2E04C1Q84295669-6C6F3E63-8F98-4140-808E-F1CB4FF446B4Q87453715-BD3EB1EA-2913-4D04-A80F-1F706C783C57Q90589781-2A10E1C5-98FD-4AF4-A419-588962AA6CC7Q91883997-F0416FD8-E7E5-4B0E-BC41-16AED354A20C
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Kristiana Gordon
@ast
Kristiana Gordon
@en
Kristiana Gordon
@es
Kristiana Gordon
@nl
type
label
Kristiana Gordon
@ast
Kristiana Gordon
@en
Kristiana Gordon
@es
Kristiana Gordon
@nl
altLabel
kristiana gordon
@en
prefLabel
Kristiana Gordon
@ast
Kristiana Gordon
@en
Kristiana Gordon
@es
Kristiana Gordon
@nl
P106
P31
P496
0000-0002-7840-5644