Lando G - Search Results

1

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S. Battistini S, et al. Among authors: lando g. J Neurol. 2005 Jul;252(7):782-8. doi: 10.1007/s00415-005-0742-y. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789135

2

Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.

Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S. Battistini S, et al. Among authors: lando g. Arch Neurol. 2007 Jun;64(6):843-8. doi: 10.1001/archneur.64.6.843. Arch Neurol. 2007. PMID: 17562932

3

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

Lando G, Mosca A, Bonora R, Azzario F, Penco S, Marocchi A, Panteghini M, Patrosso MC. Lando G, et al. Pharmacogenetics. 2003 May;13(5):265-70. doi: 10.1097/00008571-200305000-00005. Pharmacogenetics. 2003. PMID: 12724618

4

Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.

Patrosso MC, Lando G, Penco S. Patrosso MC, et al. Among authors: lando g. Hum Genet. 2008 Oct;124(3):294. Hum Genet. 2008. PMID: 18846608 No abstract available.

5

HLA-DRB1*15 association with multiple sclerosis is confirmed in a multigenerational Italian family.

Mosca L, Mantero V, Penco S, La Mantia L, De Benedetti S, Marazzi MR, Spreafico C, Erminio C, Grassi L, Lando G, Zagaria M, Agostoni E, Protti A. Mosca L, et al. Among authors: lando g. Funct Neurol. 2017 Apr/Jun;32(2):83-88. doi: 10.11138/fneur/2017.32.2.083. Funct Neurol. 2017. PMID: 28676141 Free PMC article.

6

A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of kappa light chains.

Bergström J, Patrosso MC, Colussi G, Salvadore M, Penco S, Lando G, Marocchi A, Ueda A, Nakamura M, Ando Y. Bergström J, et al. Among authors: lando g. Amyloid. 2007 Jun;14(2):141-5. doi: 10.1080/13506120701259895. Amyloid. 2007. PMID: 17577687

7

Assay using succinyldithiocholine as substrate: the method of choice for the measurement of cholinesterase catalytic activity in serum to diagnose succinyldicholine sensitivity.

Mosca A, Bonora R, Ceriotti F, Franzini C, Lando G, Patrosso MC, Zaninotto M, Panteghini M; Italian Society of Clinical Biochemistry and Clinical Molecular Biology Working Group on Enzymes. Mosca A, et al. Among authors: lando g. Clin Chem Lab Med. 2003 Mar;41(3):317-22. doi: 10.1515/CCLM.2003.051. Clin Chem Lab Med. 2003. PMID: 12705341

8

Bilateral carcinoma in situ of the testis and cystic fibrosis transmembrane conductance regulator (CFTR) mutation in an azoospermic patient with late-onset 21beta-hydroxylase deficiency.

Foppiani L, Baffico M, Lando G, Cappi C, De Cassan P, Patrosso MC, Vitali A, Penco S, Giusti M, Minuto F. Foppiani L, et al. Among authors: lando g. J Endocrinol Invest. 2004 Apr;27(4):370-4. doi: 10.1007/BF03351065. J Endocrinol Invest. 2004. PMID: 15233559

9

Effect of incremental doses of folate on homocysteine and metabolically related vitamin concentrations in nondiabetic patients on peritoneal dialysis.

de Vecchi AF, Novembrino C, Patrosso MC, Cresseri D, Ippolito S, Rosina M, Colucci P, Lando G, Bamonti Catena F. de Vecchi AF, et al. Among authors: lando g. ASAIO J. 2003 Nov-Dec;49(6):655-9. doi: 10.1097/01.mat.0000094486.12329.6b. ASAIO J. 2003. PMID: 14655730 Clinical Trial.

10

Homocysteine, vitamin B12, serum and erythrocyte folate in peritoneal dialysis patients.

De Vecchi AF, Bamonti-Catena F, Finazzi S, Patrosso C, Taioli E, Novembrino C, Colucci P, Lando G, De Franceschi M, Marocchi A, Maiolo AT. De Vecchi AF, et al. Among authors: lando g. Clin Nephrol. 2001 Apr;55(4):313-7. Clin Nephrol. 2001. PMID: 11334318

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