Berti G - Search Results

1

Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1.

Gambelli S, Malandrini A, Berti G, Gaudiano C, Zicari E, Brunori P, Perticoni G, Orrico A, Galli L, Sorrentino V, Lunardi J, Federico A, Dotti MT. Gambelli S, et al. Among authors: berti g. Clin Genet. 2007 Jan;71(1):93-4. doi: 10.1111/j.1399-0004.2006.00725.x. Clin Genet. 2007. PMID: 17204054 No abstract available.

2

Neuropathological findings associated with retained lead shot pellets in a man surviving two months after a suicide attempt.

Malandrini A, Villanova M, Salvadori C, Gambelli S, Berti G, Di Paolo M. Malandrini A, et al. Among authors: berti g. J Forensic Sci. 2001 May;46(3):717-21. J Forensic Sci. 2001. PMID: 11373015

3

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.

Malandrini A, Mari F, Palmeri S, Gambelli S, Berti G, Bruttini M, Bardelli AM, Williamson K, van Heyningen V, Renieri A. Malandrini A, et al. Among authors: berti g. Clin Genet. 2001 Aug;60(2):151-4. doi: 10.1034/j.1399-0004.2001.600210.x. Clin Genet. 2001. PMID: 11553050

4

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

Malandrini A, Ceuterick C, Villanova M, Gambelli S, Berti G, Rossi A, Guazzi GC. Malandrini A, et al. Among authors: berti g. J Submicrosc Cytol Pathol. 2001 Jan-Apr;33(1-2):59-63. J Submicrosc Cytol Pathol. 2001. PMID: 11686409

5

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL.

Malandrini A, Albani F, Palmeri S, Fattapposta F, Gambelli S, Berti G, Bracco A, Tammaro A, Calzavara S, Villanova M, Ferrari M, Rossi A, Carrera P. Malandrini A, et al. Among authors: berti g. Neurology. 2002 Aug 27;59(4):617-20. doi: 10.1212/wnl.59.4.617. Neurology. 2002. PMID: 12196662

6

Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular dystrophy.

Gambelli S, Malandrini A, Ginanneschi F, Berti G, Cardaioli E, De Stefano R, Franci M, Salvadori C, Mari F, Bruttini M, Rossi A, Federico A, Renieri A. Gambelli S, et al. Among authors: berti g. Eur Neurol. 2004;51(3):144-7. doi: 10.1159/000077070. Epub 2004 Feb 27. Eur Neurol. 2004. PMID: 14988608

7

DNA end labelling (TUNEL) in a 3 year old girl with Leigh syndrome and prevalent cortical involvement.

Formichi P, Malandrini A, Battisti C, Santorelli FM, Gambelli S, Tripodi SA, Berti G, Salvadori C, Tessa A, Federico A. Formichi P, et al. Among authors: berti g. J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):930-2. doi: 10.1136/jnnp.2003.016410. J Neurol Neurosurg Psychiatry. 2004. PMID: 15146020 Free PMC article.

8

A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course.

Malandrini A, Luchini D, Gambelli S, Gaudiano C, Berti G, Salvadori C, Serni G, Valassina M, Federico A, Di Paolo M. Malandrini A, et al. Among authors: berti g. J Clin Forensic Med. 2004 Aug;11(4):208-10. doi: 10.1016/j.jcfm.2004.04.009. J Clin Forensic Med. 2004. PMID: 15363755

9

Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype.

Malandrini A, Gambelli S, Muglia M, Berti G, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: berti g. Neurology. 2005 Sep 13;65(5):776. doi: 10.1212/01.wnl.0000174516.41417.b9. Neurology. 2005. PMID: 16157924 No abstract available.

10

Typical pathological changes of CADASIL in the optic nerve.

Rufa A, Malandrini A, Dotti MT, Berti G, Salvadori C, Federico A. Rufa A, et al. Among authors: berti g. Neurol Sci. 2005 Oct;26(4):271-4. doi: 10.1007/s10072-005-0470-1. Neurol Sci. 2005. PMID: 16193254

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