Michelini S - Search Results

1

Proprioception sense in lymphedema affected upper limb.

Cardone M, Cappellino F, Vincenzo S, Moneta G, Failla A, Iosa M, Monni B, Fantegrossi MR, Rubeghi V, Michelini S. Cardone M, et al. Among authors: michelini s. Lymphology. 2018;51(2):66-72. Lymphology. 2018. PMID: 30253457

2

Melilotus, Rutin and Bromelain in primary and secondary lymphedema.

Michelini S, Fiorentino A, Cardone M. Michelini S, et al. Lymphology. 2019;52(4):177-186. Lymphology. 2019. PMID: 32171184

3

[National epidemiologic study of lymphedema].

Michelini S, Campisi C, Cavezzi A, Boccardo F, Failla A, Moneta G. Michelini S, et al. Minerva Cardioangiol. 1998 Oct;46(10):393-4. Minerva Cardioangiol. 1998. PMID: 10021824 Italian. No abstract available.

4

[Combination treatment of lymphedema. Our experience].

Michelini S, Campisi C, Failla A, Boccardo F, Moneta G. Michelini S, et al. Minerva Cardioangiol. 1998 Oct;46(10):395-6. Minerva Cardioangiol. 1998. PMID: 10021825 Italian. No abstract available.

5

Clinical and genetic study of 46 Italian patients with primary lymphedema.

Michelini S, Degiorgio D, Cestari M, Corda D, Ricci M, Cardone M, Mander A, Famoso L, Contini E, Serrani R, Pinelli L, Cecchin S, Bertelli M. Michelini S, et al. Lymphology. 2012 Mar;45(1):3-12. Lymphology. 2012. PMID: 22768468

6

Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.

Michelini S, Vettori A, Maltese PE, Cardone M, Bruson A, Fiorentino A, Cappellino F, Sainato V, Guerri G, Marceddu G, Tezzele S, Bertelli M. Michelini S, et al. Lymphology. 2016 Jun;49(2):57-72. Lymphology. 2016. PMID: 29906362

7

[Study on the efficacy of ginkgo biloba extract, magnesium and levo-arginine in the treatment of patients with 2d stage arteriopathies. A preliminary study].

Michelini S, Micci A, Failla A, Moneta G, Ottaviani A. Michelini S, et al. Minerva Cardioangiol. 1998 Sep;46(9):319-20. Minerva Cardioangiol. 1998. PMID: 10021862 Clinical Trial. Italian. No abstract available.

8

A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene.

Michelini S, Cardone M, Haag M, Agga O, Bruson A, Maltese PE, Bonizzato A, Bertelli M. Michelini S, et al. Lymphology. 2016 Mar;49(1):15-20. Lymphology. 2016. PMID: 29906059

9

[Clinical experience in patients with chronic peripheral obliterating arteriopathy: defibrotide versus definite molecular weight heparan sulfate (MW 7500-15000 dalton)].

Michelini S, Micci A, Failla A, Grechi G, Iantaffi A. Michelini S, et al. Minerva Cardioangiol. 1996 Jan-Feb;44(1-2):33-7. Minerva Cardioangiol. 1996. PMID: 8767620 Clinical Trial. Italian.

10

Rare PECAM1 variants in three families with lymphedema.

Michelini S, Amato B, Kenanoglu S, Veselenyiova D, Dautaj A, Kurti D, Baglivo M, Dundar M, Krajcovic J, Miggiano GA, Aquilanti B, Matera G, Velluti V, Gagliardi L, Basha SH, Bertelli M. Michelini S, et al. Lymphology. 2020;53(3):141-151. Lymphology. 2020. PMID: 33350288

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