Panza E - Search Results

1

Benign albeit glycolytic: MCT4 expression and lactate release in giant cell tumour of bone.

Avnet S, Lemma S, Errani C, Falzetti L, Panza E, Columbaro M, Nanni C, Baldini N. Avnet S, et al. Among authors: panza e. Bone. 2020 May;134:115302. doi: 10.1016/j.bone.2020.115302. Epub 2020 Feb 26. Bone. 2020. PMID: 32112988

2

Application of a fluorescent PCR method for molecular diagnosis of posttransplant lymphoproliferative disorders on routine tissue sections.

Gruppioni E, Corti B, Altimari A, Gabusi E, Panza E, Grazi GL, Pinna AD, De Ruvo N, Fiorentino M, Grigioni WF, Grigioni AD. Gruppioni E, et al. Among authors: panza e. Diagn Mol Pathol. 2005 Sep;14(3):170-6. doi: 10.1097/01.pas.0000162756.84026.44. Diagn Mol Pathol. 2005. PMID: 16106199

3

Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle Metabolism.

Panza E, Martinelli D, Magini P, Dionisi Vici C, Seri M. Panza E, et al. Front Neurol. 2019 Feb 22;10:131. doi: 10.3389/fneur.2019.00131. eCollection 2019. Front Neurol. 2019. PMID: 30853934 Free PMC article. Review.

4

Phenotypic Description of A Patient with ODLURO Syndrome and Functional Characterization of the Pathogenetic Role of A Synonymous Variant c.186G>A in KMT2E Gene.

Benvenuto M, Cesarini S, Severi G, Ambrosini E, Russo A, Seri M, Palumbo P, Palumbo O, Castori M, Panza E, Carella M. Benvenuto M, et al. Among authors: panza e. Genes (Basel). 2024 Mar 29;15(4):430. doi: 10.3390/genes15040430. Genes (Basel). 2024. PMID: 38674365 Free PMC article.

5

ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

Panza E, Escamilla-Honrubia JM, Marco-Marín C, Gougeard N, De Michele G, Morra VB, Liguori R, Salviati L, Donati MA, Cusano R, Pippucci T, Ravazzolo R, Németh AH, Smithson S, Davies S, Hurst JA, Bordo D, Rubio V, Seri M. Panza E, et al. Brain. 2016 Jan;139(Pt 1):e3. doi: 10.1093/brain/awv247. Epub 2015 Aug 21. Brain. 2016. PMID: 26297558 No abstract available.

6

The clear cell sarcoma functional genomic landscape.

Panza E, Ozenberger BB, Straessler KM, Barrott JJ, Li L, Wang Y, Xie M, Boulet A, Titen SW, Mason CC, Lazar AJ, Ding L, Capecchi MR, Jones KB. Panza E, et al. J Clin Invest. 2021 Aug 2;131(15):e146301. doi: 10.1172/JCI146301. J Clin Invest. 2021. PMID: 34156976 Free PMC article.

7

Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanisms.

Martinello C, Panza E, Orlacchio A. Martinello C, et al. Among authors: panza e. Expert Rev Proteomics. 2023 Jul-Dec;20(7-9):171-188. doi: 10.1080/14789450.2023.2260952. Epub 2023 Oct 16. Expert Rev Proteomics. 2023. PMID: 37788157 Review.

8

Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation.

Graziano C, Carone S, Panza E, Marino F, Magini P, Romeo G, Pession A, Seri M. Graziano C, et al. Among authors: panza e. Blood. 2009 Aug 20;114(8):1655-7. doi: 10.1182/blood-2009-04-217851. Epub 2009 Jun 24. Blood. 2009. PMID: 19553636 Free article.

9

Pecci A, Panza E, De Rocco D, Pujol-Moix N, Girotto G, Podda L, Paparo C, Bozzi V, Pastore A, Balduini CL, Seri M, Savoia A. Pecci A, et al. Among authors: panza e. Eur J Haematol. 2010 Apr;84(4):291-7. doi: 10.1111/j.1600-0609.2009.01398.x. Epub 2009 Dec 11. Eur J Haematol. 2010. PMID: 20002731 Clinical Trial.

10

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

Savoia A, De Rocco D, Panza E, Bozzi V, Scandellari R, Loffredo G, Mumford A, Heller PG, Noris P, De Groot MR, Giani M, Freddi P, Scognamiglio F, Riondino S, Pujol-Moix N, Fabris F, Seri M, Balduini CL, Pecci A. Savoia A, et al. Among authors: panza e. Thromb Haemost. 2010 Apr;103(4):826-32. doi: 10.1160/TH09-08-0593. Epub 2010 Feb 19. Thromb Haemost. 2010. PMID: 20174760

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