1. bookVolume 1 (2017): Edition s2 (December 2017)
    MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
Détails du magazine
License
Format
Magazine
eISSN
2564-615X
Première parution
30 Jan 2017
Périodicité
4 fois par an
Langues
Anglais
Accès libre

Primary lymphedema and genetic implications

Publié en ligne: 28 Dec 2017
Volume & Edition: Volume 1 (2017) - Edition s2 (December 2017) - MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
Pages: 144 - 146
Détails du magazine
License
Format
Magazine
eISSN
2564-615X
Première parution
30 Jan 2017
Périodicité
4 fois par an
Langues
Anglais

1. Northup KA, Witthe MH, Witte CL. Syndromic classification of hereditary lymphedema. Lymphology 2003; 36: 162-189.Search in Google Scholar

2. Connell F, Brice G, Jeffery S, Keele YV, Mortimer P, Smansour S. A new classification system for primary lymphatic dysplasias based on phenotype. Clin Gen 2010; 77 (5): 438-452.10.1111/j.1399-0004.2010.01394.x20447153Search in Google Scholar

3 . Adams RH, Alitalo K. Molecular regulation of angiogenesis and lymphangiogenesis. Nat Rev Mol Cell Biol 2007; 8 (6): 464-47810.1038/nrm218317522591Ouvrir le DOISearch in Google Scholar

4. Alitalo K, Karkkainen M: VEGF-C and VEGF-D growth factor therapy for lymphedema. Abstract book of XIX international congress of Lymphology. Friburgo, 1-6 settembre 2003.Search in Google Scholar

5. Lee B., Andrade M., Bergan J., Boccardo F., Campisi C., Damstra R., Flour M., Gloviczki P., Laredo J., Piller N., Michelini S., Mortimer P., Villavicencio J. L.. Diagnosis and treatment of primary lymphedema. Consensus Document of the International Union of Phlebology (IUP)-2009. International Angiology 2010; 29(5):454-70.Search in Google Scholar

6. Lee BB, Antignani PL, Baroncelli TA, Boccardo FM, Brorson H, Campisi C, Damstra RJ, Flour M, Giannoukas A, Laredo J, Liu NF, Michelini S, Piller N, Rockson SG, Scuderi A, Szolnojy G, Yamamoto T IUA-ISVI Consensus for Diagnosis Guideline of chronic lymphedema of the limbs. Int Angiol 2014;18.Search in Google Scholar

7. Michelini S, Vettori A, Maltese PE, Cardone M, Bruson A, Fiorentino A, Cappellino F, Sainato V, Guerri G, Marceddu G, Tezzele S, Bertelli M. Genetic screening in a large cohort of Italian patients affected by primary lymphedema using next generation sequencing (NGS) approach. Lymphology 2016; 29: 57-72.Search in Google Scholar

8. Michelini S, De Giorgio D, Cestari M, Corda D, Ricci M, Cardone M, et al. Clinical and genetic study of 46 italian patients with primary lymphedema. Lymphology 2012; 45: 3-12.Search in Google Scholar

9. Michelini S, Bruson A, Cardone F, Sirocco A, Fiorentino S, Cecchin S, Cappellino F, Bertelli M. Clinical and genetic assessment of primary lymphedema. Lymphology 47: 19-24. Rome 2015-09-24Search in Google Scholar

10. Ferrel RE, Levinson KL, Esman JH, Komak MA, Lawrence EC, Barmada MM, Finegold DN. Hereditary lymphedema evidence for linkage and genetic heterogeneity. Hum Mol Genet 1998 ; 7 (13): 2073-8.10.1093/hmg/7.13.20739817924Search in Google Scholar

11. Michelini S, Cardone M, Haag O, Agga M, Bruson A, Maltese PE, Bonizzato A, Bertelli MA rare case of Emberger syndrome caused by a de novo mtutation in the GATA2 gene. Lymphology 2016; 49:15-20.Search in Google Scholar

Articles recommandés par Trend MD

Planifiez votre conférence à distance avec Sciendo