Banchini G - Search Results

1

Dermatologic features in Pallister-Killian syndrome and their importance to the diagnosis.

Guareschi E, Garavelli L, Pedori S, Di Lernia V, Grenzi L, Franchi F, Marinelli M, Croci GF, Pedretti E, Amarri S, Banchini G, Albertini G. Guareschi E, et al. Among authors: banchini g. Pediatr Dermatol. 2007 Jul-Aug;24(4):426-8. doi: 10.1111/j.1525-1470.2007.00469.x. Pediatr Dermatol. 2007. PMID: 17845177 No abstract available.

2

MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature.

Garavelli L, Leask K, Zanacca C, Pedori S, Albertini G, Della Giustina E, Croci GF, Magnani C, Banchini G, Clayton-Smith J, Bocian M, Firth H, Gold JA, Hurst J. Garavelli L, et al. Among authors: banchini g. Genet Couns. 2005;16(2):117-28. Genet Couns. 2005. PMID: 16080291

3

Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review.

Garavelli L, Cerruti-Mainardi P, Virdis R, Pedori S, Pastore G, Godi M, Provera S, Rauch A, Zweier C, Zollino M, Banchini G, Longo N, Mowat D, Neri G, Bernasconi S. Garavelli L, et al. Among authors: banchini g. Horm Res. 2005;63(4):187-92. doi: 10.1159/000085894. Epub 2005 May 20. Horm Res. 2005. PMID: 15908750

4

Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review.

Garavelli L, Pedori S, Dal Zotto R, Franchi F, Marinelli M, Croci GF, Bellato S, Ammenti A, Virdis R, Banchini G, Superti-Furga A. Garavelli L, et al. Among authors: banchini g. Genet Couns. 2006;17(4):449-55. Genet Couns. 2006. PMID: 17375532 Review.

5

Oculo-auriculo-vertebral spectrum in Klinefelter syndrome.

Garavelli L, Virdis R, Donadio A, Sigorini M, Banchini G, Balestrazzi P, Fryns JP. Garavelli L, et al. Among authors: banchini g. Genet Couns. 1999;10(3):321-4. Genet Couns. 1999. PMID: 10546106

6

Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1.

Garavelli L, Pedori S, Zanacca C, Caselli G, Loiodice A, Mantovani G, Ammenti A, Virdis R, Banchini G. Garavelli L, et al. Among authors: banchini g. Acta Biomed. 2005 Apr;76(1):45-8. Acta Biomed. 2005. PMID: 16116826

7

Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new case.

Garavelli L, Guareschi E, Errico S, Simoni A, Bergonzini P, Zollino M, Gurrieri F, Mancini GM, Schot R, Van Der Spek PJ, Frigieri G, Zonari P, Albertini E, Giustina ED, Amarri S, Banchini G, Dobyns WB, Neri G. Garavelli L, et al. Among authors: banchini g. Neuropediatrics. 2007 Aug;38(4):200-3. doi: 10.1055/s-2007-985908. Neuropediatrics. 2007. PMID: 18058629

8

[Care recommendations for type 1 neurofibromatosis].

Donadio A, Garavelli L, Lorenzetti ME, Villani AR, Banchini G, Virdis R. Donadio A, et al. Among authors: banchini g. Acta Biomed Ateneo Parmense. 2000;71(3-4):83-7. Acta Biomed Ateneo Parmense. 2000. PMID: 11424620 Italian.

9

[Genetics of type 1 neurofibromatosis].

Garavelli L, Donadio A, Sigorini M, Grassi L, Banchini G. Garavelli L, et al. Among authors: banchini g. Acta Biomed Ateneo Parmense. 2000;71(3-4):89-95. Acta Biomed Ateneo Parmense. 2000. PMID: 11424621 Italian.

10

Marden-Walker syndrome: case report, nosologic discussion and aspects of counseling.

Garavelli L, Donadio A, Banchini G, Magnani C, Magnani C, Calzolari E, Fryns JP. Garavelli L, et al. Among authors: banchini g. Genet Couns. 2000;11(2):111-8. Genet Couns. 2000. PMID: 10893662

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