E-LIB Suche - Ergebnisse für: Ricca, I.

1

New CACNA1A deletions are associated to migraine phenotypes:

Grieco, G. S. ; Gagliardi, S. ; Ricca, I....
The Journal of Headache and Pain. 19 (2018) 1 - p. , 2018

Link: https://doi.org/10.1186/..

2

Palmoplantar keratoderma and Charcot-Marie-Tooth disease: c..:

Gagliardi, S. ; Ricca, I. ; Ferrarini, A....
British Journal of Dermatology. 177 (2017) 1 - p. 284-286 , 2017

Link: https://doi.org/10.1111/..

3

C011 Marked telomere loss following autologous stem cell tr..:

Ricca, I. ; Rocci, A. ; Zanni, M....
Leukemia Research. 31 (2007) - p. S28-S29 , 2007

Link: https://doi.org/10.1016/..

4

Rituximab anti-CD20 monoclonal antibody induces marked but ..:

Ladetto, M ; Bergui, L ; Ricca, I...
Medical Oncology. 17 (2000) 3 - p. 203-210 , 2000

Link: https://doi.org/10.1007/..

5

Tissue Inhibitor of Metalloproteinase 1 Expression Associat..:

Ricca, Tatiana I. ; Liang, Gangning ; Suenaga, Ana Paula M....
Translational Oncology. 2 (2009) 4 - p. 329-340 , 2009

Link: https://doi.org/10.1593/..

6

Melanocyte Transformation Associated with Substrate Adhesio..:

Oba-Shinjo, Sueli M. ; Correa, Mariangela ; Ricca, Tatiana I....
Neoplasia. 8 (2006) 3 - p. 231-241 , 2006

Link: https://doi.org/10.1593/..

7

Diagnosis and treatment of chronic synovitis in patients wi..:

Di Minno M. N. D ; Napolitano M ; Giuffrida A. C...
info:eu-repo/semantics/altIdentifier/pmid/34923621. , 2022

Link: http://hdl.handle.net/11..

8

Clinical-Genetic Features Influencing Disability in Spastic..:

Rossi S ; Rubegni A ; Riso V...
info:eu-repo/semantics/altIdentifier/pmid/35372684. , 2022

Link: http://hdl.handle.net/11..

9

Clinical-Genetic Features Influencing Disability in Spastic..:

Rossi S ; Rubegni A ; Riso V...
info:eu-repo/semantics/altIdentifier/pmid/35372684. , 2022

Link: https://hdl.handle.net/1..

10

Episodic ataxia and severe infantile phenotype in spinocere..:

De Michele G ; Galatolo D ; Galosi S...
info:eu-repo/semantics/altIdentifier/pmid/34292398. , 2022

Link: http://hdl.handle.net/11..

11

Intracranial Haemorrhage in Haemophilia Patients Is Still a..:

Zanon E ; Pasca S ; Demartis F...
info:eu-repo/semantics/altIdentifier/wos/WOS:000780505300001. , 2022

Link: http://hdl.handle.net/11..

12

Episodic ataxia and severe infantile phenotype in spinocere..:

De Michele G ; Galatolo D ; Galosi S...
info:eu-repo/semantics/altIdentifier/wos/WOS:000675768200002. , 2022

Link: https://hdl.handle.net/1..

13

Erratum: Biallelic variants in HPDL cause pure and complica..:

Wiessner M ; Maroofian R ; Ni M. -Y...
info:eu-repo/semantics/altIdentifier/wos/WOS:000710930500006. , 2021

Link: https://hdl.handle.net/1..

14

Ngs in hereditary ataxia: When rare becomes frequent:

Galatolo D ; De Michele G ; Silvestri G...
info:eu-repo/semantics/altIdentifier/pmid/34445196. , 2021

Link: http://hdl.handle.net/11..

15

De novo 1q21.3q22 duplication revaluation in a "cold" compl..:

Milone R ; Scalise R ; Pasquariello R...
info:eu-repo/semantics/altIdentifier/pmid/33807234. , 2021

Link: http://hdl.handle.net/11..