Gobbi G - Search Results

1

Hypomelanosis of Ito with trisomy 18 mosaicism.

Grazia R, Tullini A, Rossi PG, Neri I, Patrizi A, Croci G, Manenti E, Gobbi G. Grazia R, et al. Among authors: gobbi g. Am J Med Genet. 1993 Jan 1;45(1):120-1. doi: 10.1002/ajmg.1320450134. Am J Med Genet. 1993. PMID: 8418648 No abstract available.

2

[Sebaceous linear nevus syndrome with hemimegalencephaly. Report of a case].

Patrizi A, Pizzino D, Tullini A, Gobbi G, Santucci M. Patrizi A, et al. Among authors: gobbi g. G Ital Dermatol Venereol. 1989 Jan-Feb;124(1-2):55-8. G Ital Dermatol Venereol. 1989. PMID: 2767720 Italian.

3

Familial Unverricht-Lundborg disease: a clinical, neurophysiologic, and genetic study.

Parmeggiani A, Lehesjoki AE, Carelli V, Posar A, Santi A, Santucci M, Gobbi G, Pini A, Rossi PG. Parmeggiani A, et al. Among authors: gobbi g. Epilepsia. 1997 Jun;38(6):637-41. doi: 10.1111/j.1528-1157.1997.tb01232.x. Epilepsia. 1997. PMID: 9186245 Free article.

4

Occipital seizures in Lafora disease: a further case documented by EEG.

Tinuper P, Gobbi G, Aguglia U, Rossi PG, Lugaresi E. Tinuper P, et al. Among authors: gobbi g. Clin Electroencephalogr. 1985 Jul;16(3):167-70. doi: 10.1177/155005948501600312. Clin Electroencephalogr. 1985. PMID: 3930106

5

Epilepsy with bilateral occipital calcifications: a benign onset with progressive severity.

Gobbi G, Sorrenti G, Santucci M, Rossi PG, Ambrosetto P, Michelucci R, Tassinari CA. Gobbi G, et al. Neurology. 1988 Jun;38(6):913-20. doi: 10.1212/wnl.38.6.913. Neurology. 1988. PMID: 3368073

6

[Sjogren-Larsson syndrome. Contribution to an early diagnosis].

Patrizi A, Varotti C, Gobbi G, Romeo G, Gualdi Russo E, Giovanardi Rossi P. Patrizi A, et al. Among authors: gobbi g. G Ital Dermatol Venereol. 1983 Jan-Feb;118(1):17-20. G Ital Dermatol Venereol. 1983. PMID: 6642556 Italian. No abstract available.

7

Severe epilepsy preceding by four months the onset of scleroderma en coup de sabre.

Sartori S, Martini G, Calderone M, Patrizi A, Gobbi G, Zulian F. Sartori S, et al. Among authors: gobbi g. Clin Exp Rheumatol. 2009 May-Jun;27(3 Suppl 54):64-7. Clin Exp Rheumatol. 2009. PMID: 19796565

8

Chromosome 18 aberrations and epilepsy: a review.

Grosso S, Pucci L, Di Bartolo RM, Gobbi G, Bartalini G, Anichini C, Scarinci R, Balestri M, Farnetani MA, Cioni M, Morgese G, Balestri P. Grosso S, et al. Among authors: gobbi g. Am J Med Genet A. 2005 Apr 1;134A(1):88-94. doi: 10.1002/ajmg.a.30575. Am J Med Genet A. 2005. PMID: 15690352

9

"Minimal" holoprosencephaly in a 14q deletion syndrome patient.

Della Giustina E, Iodice A, Spagnoli C, Giovannini S, Frattini D, Fusco C, Gobbi G, Zollino M, Neri G. Della Giustina E, et al. Among authors: gobbi g. Am J Med Genet A. 2017 Dec;173(12):3216-3220. doi: 10.1002/ajmg.a.38378. Am J Med Genet A. 2017. PMID: 29136354

10

Neuropsychological findings: myoclonic astatic epilepsy (MAE) and Lennox-Gastaut syndrome (LGS).

Filippini M, Boni A, Dazzani G, Guerra A, Gobbi G. Filippini M, et al. Among authors: gobbi g. Epilepsia. 2006;47 Suppl 2:56-9. doi: 10.1111/j.1528-1167.2006.00691.x. Epilepsia. 2006. PMID: 17105463 Free article.

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