Banchini G - Search Results

1

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

2

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

3

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

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

[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.

6

[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.

7

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

8

Kabuki syndrome and diaphragmatic defects: a frequent association in non-Asian patients?

Donadio A, Garavelli L, Banchini G, Neri G. Donadio A, et al. Among authors: banchini g. Am J Med Genet. 2000 Mar 13;91(2):164-5. Am J Med Genet. 2000. PMID: 10748421 No abstract available.

9

Mandibuloacral dysplasia type A in childhood.

Garavelli L, D'Apice MR, Rivieri F, Bertoli M, Wischmeijer A, Gelmini C, De Nigris V, Albertini E, Rosato S, Virdis R, Bacchini E, Dal Zotto R, Banchini G, Iughetti L, Bernasconi S, Superti-Furga A, Novelli G. Garavelli L, et al. Among authors: banchini g. Am J Med Genet A. 2009 Oct;149A(10):2258-64. doi: 10.1002/ajmg.a.33005. Am J Med Genet A. 2009. PMID: 19764019

10

Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.

Garavelli L, Zanacca C, Caselli G, Banchini G, Dubourg C, David V, Odent S, Gurrieri F, Neri G. Garavelli L, et al. Among authors: banchini g. Am J Med Genet A. 2004 May 15;127A(1):93-95. doi: 10.1002/ajmg.a.20685. Am J Med Genet A. 2004. PMID: 15103725

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