Gurrieri F - Search Results

1

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: gurrieri f. Neuropediatrics. 2007 Aug;38(4):200-3. doi: 10.1055/s-2007-985908. Neuropediatrics. 2007. PMID: 18058629

2

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: gurrieri f. 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

3

Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.

Garavelli L, Zollino M, Mainardi PC, Gurrieri F, Rivieri F, Soli F, Verri R, Albertini E, Favaron E, Zignani M, Orteschi D, Bianchi P, Faravelli F, Forzano F, Seri M, Wischmeijer A, Turchetti D, Pompilii E, Gnoli M, Cocchi G, Mazzanti L, Bergamaschi R, De Brasi D, Sperandeo MP, Mari F, Uliana V, Mostardini R, Cecconi M, Grasso M, Sassi S, Sebastio G, Renieri A, Silengo M, Bernasconi S, Wakamatsu N, Neri G. Garavelli L, et al. Among authors: gurrieri f. Am J Med Genet A. 2009 Mar;149A(3):417-26. doi: 10.1002/ajmg.a.32693. Am J Med Genet A. 2009. PMID: 19215041 Review.

4

An additional patient with the 3C syndrome.

Gurrieri F, Neri G. Gurrieri F, et al. Clin Genet. 1992 May;41(5):263-5. doi: 10.1111/j.1399-0004.1992.tb03678.x. Clin Genet. 1992. PMID: 1606716

5

Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome.

Gurrieri F, Scarano G, Garavelli L, Della Monica M, Lonardo F, Cuda D, Banchini G, Opitz JM, Neri G. Gurrieri F, et al. Am J Med Genet A. 2004 Apr 15;126A(2):204-7. doi: 10.1002/ajmg.a.20575. Am J Med Genet A. 2004. PMID: 15057987

6

Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome.

Tabolacci E, Zollino M, Lecce R, Sangiorgi E, Gurrieri F, Leuzzi V, Opitz JM, Neri G. Tabolacci E, et al. Among authors: gurrieri f. Clin Dysmorphol. 2005 Jul;14(3):127-132. Clin Dysmorphol. 2005. PMID: 15930901

7

Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.

Gurrieri F, Cappa M, Neri G. Gurrieri F, et al. Am J Med Genet. 1992 Sep 15;44(2):136-7. doi: 10.1002/ajmg.1320440203. Am J Med Genet. 1992. PMID: 1456280

8

Defective oxytocin function: a clue to understanding the cause of autism?

Gurrieri F, Neri G. Gurrieri F, et al. BMC Med. 2009 Oct 22;7:63. doi: 10.1186/1741-7015-7-63. BMC Med. 2009. PMID: 19845973 Free PMC article.

9

New syndrome of mental retardation, Robin sequence, and brachydactyly.

Gurrieri F, Steindl K, Giglio S, Neri G. Gurrieri F, et al. Am J Med Genet. 2001 Apr 15;100(1):49-51. doi: 10.1002/1096-8628(20010415)100:1<49::aid-ajmg1213>3.0.co;2-v. Am J Med Genet. 2001. PMID: 11337748

10

A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer.

Lucci-Cordisco E, Zollino M, Baglioni S, Mancuso I, Lecce R, Gurrieri F, Crucitti A, Papi L, Neri G, Genuardi M. Lucci-Cordisco E, et al. Among authors: gurrieri f. Clin Genet. 2005 Feb;67(2):178-82. doi: 10.1111/j.1399-0004.2004.00390.x. Clin Genet. 2005. PMID: 15679831

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