1. bookTom 1 (2017): Zeszyt s2 (December 2017)
    MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
Informacje o czasopiśmie
License
Format
Czasopismo
eISSN
2564-615X
Pierwsze wydanie
30 Jan 2017
Częstotliwość wydawania
4 razy w roku
Języki
Angielski
Otwarty dostęp

Primary lymphedema and genetic implications

Data publikacji: 28 Dec 2017
Tom & Zeszyt: Tom 1 (2017) - Zeszyt s2 (December 2017) - MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
Zakres stron: 144 - 146
Informacje o czasopiśmie
License
Format
Czasopismo
eISSN
2564-615X
Pierwsze wydanie
30 Jan 2017
Częstotliwość wydawania
4 razy w roku
Języki
Angielski

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/nrm218317522591Otwórz 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

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