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au.\*:("CASTORI, Marco")

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Results 1 to 25 of 47

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Genetic skin diseases predisposing to basal cell carcinomaCASTORI, Marco; MORRONE, Aldo; KANITAKIS, Jean et al.EJD. European journal of dermatology. 2012, Vol 22, Num 3, pp 299-309, issn 1167-1122, 11 p.Article

Bazex-Dupré-Christol syndrome: An ectodermal dysplasia with skin appendage neoplasmsCASTORI, Marco; CASTIGLIA, Daniele; PASSARELLI, Francesca et al.European journal of medical genetics. 2009, Vol 52, Num 4, pp 250-255, issn 1769-7212, 6 p.Article

Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke : Clinical report and review of cerebral vascular anomaliesBRANCATI, Francesco; CASTORI, Marco; MINGARELLI, Rita et al.American journal of medical genetics. 2005, Vol 139A, Num 3, pp 212-215, issn 0148-7299, 4 p.Article

Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvansCASTORI, Marco; COVACIU, Claudia; PARADISI, Mauro et al.European journal of medical genetics. 2009, Vol 52, Num 1, pp 53-58, issn 1769-7212, 6 p.Article

Tibial Developmental Field Defect Is the Most Common Lower Limb Malformation Pattern in VACTERL AssociationCASTORI, Marco; RINALDI, Rosanna; CAPPELLACCI, Sandra et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 10, pp 1259-1266, issn 1552-4825, 8 p.Article

The Nosology of Richieri-Costa/Guion-Almeida Syndrome(s)CASTORI, Marco; CASCONE, Piero; BRINELLI, Marco et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 398-402, issn 1552-4825, 5 p.Article

Ehlers―Danlos Syndrome Hypermobility Type and the Excess of Affected Females: Possible Mechanisms and PerspectivesCASTORI, Marco; CAMEROTA, Filippo; CELLETTI, Claudia et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 9, pp 2406-2408, issn 1552-4825, 3 p.Article

A rare cause of syndromic hypotrichosis : Nicolaides-Baraitser syndromeCASTORI, Marco; COVACIU, Claudia; RINALDI, Rosanna et al.Journal of the American Academy of Dermatology. 2008, Vol 59, Num 5, issn 0190-9622, S92-S98, SUPArticle

Schöpf-Schulz-Passarge Syndrome : Further Delineation of the Phenotype and Genetic ConsiderationsCASTORI, Marco; RUGGIERI, Salvatore; GIANNETTI, Luca et al.Acta dermato-venereologica. 2008, Vol 88, Num 6, pp 607-612, issn 0001-5555, 6 p.Article

A novel patient with cooks syndrome supports splitting from classic brachydactyly type BCASTORI, Marco; BRANCATI, Francesco; MINGARELLI, Rita et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 2, pp 195-199, issn 1552-4825, 5 p.Article

A triploid fetus further expands etiological heterogeneity in holoprosencephaly-diencephalic hamartoblastomaCASTORI, Marco; SILVESTRI, Evelina; NUNNARI, Josè et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 12, pp 1391-1393, issn 1552-4825, 3 p.Article

Palmoplantar Keratoderma, Pseudo-Ainhum, and Universal Atrichia: A New Patient and Review of the Palmoplantar Keratoderma-Congenital Alopecia SyndromeCASTORI, Marco; VALIANTE, Michele; RITELLI, Marco et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 8, pp 2043-2047, issn 1552-4825, 5 p.Article

Use of the Gait Profile Score for the evaluation of patients with joint hypermobility syndrome/Ehlers―Danlos syndrome hypermobility typeCELLETTI, Claudia; GALLI, Manuela; CIMOLIN, Veronica et al.Research in developmental disabilities (Print). 2013, Vol 34, Num 11, pp 4280-4285, issn 0891-4222, 6 p.Article

Relationship between fatigue and gait abnormality in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility typeCELLETTI, Claudia; GALLI, Manuela; CIMOLIN, Veronica et al.Research in developmental disabilities (Print). 2012, Vol 33, Num 6, pp 1914-1918, issn 0891-4222, 5 p.Article

Monozygotic Twin Discordance for Phacomatosis Cesioflammea Further Supports the Post-Zygotic Mutation HypothesisCASTORI, Marco; SARAZANI, Stefano; BINNI, Francesco et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 9, pp 2253-2256, issn 1552-4825, 4 p.Article

Functional Characterization of a Novel TP63 Mutation in a Family With Overlapping Features of Rapp-Hodgkin/AEC/ADULT SyndromesSERRA, Valeria; CASTORI, Marco; PARADISI, Mauro et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3104-3109, issn 1552-4825, 6 p.Article

Association of segmental neurofibromatosis 1 and oculo-auriculo-vertebral spectrum in a 24-year-old femaleCASTORI, Marco; MAJORE, Silvia; ROMANELLI, Francesco et al.EJD. European journal of dermatology. 2008, Vol 18, Num 1, pp 22-25, issn 1167-1122, 4 p.Article

Evaluation of Balance and Improvement of Proprioception by Repetitive Muscle Vibration in a 15-Year-Old Girl With Joint Hypermobility SyndromeCELLETTI, Claudia; CASTORI, Marco; GALLI, Manuela et al.Arthritis care and research. 2011, Vol 63, Num 5, pp 775-779, issn 0893-7524, 5 p.Article

Sirenomelia and VACTERL Association in the Offspring of a Woman With DiabetesCASTORI, Marco; SILVESTRI, Evelina; CAPPELLACCI, Sandra et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 7, pp 1803-1807, issn 1552-4825, 5 p.Article

Phacomatosis Cesioflammea With Unilateral LipohypoplasiaCASTORI, Marco; RINALDI, Rosanna; ANGELO, Corrado et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 4, pp 492-495, issn 1552-4825, 4 p.Article

Antenatal presentation of the oculo-auriculo-vertebral spectrum (OAVS)CASTORI, Marco; BRANCATI, Francesco; RINALDI, Rosanna et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 14, pp 1573-1579, issn 1552-4825, 7 p.Article

Whorled Hairless Nevus of the Scalp, Linear Hyperpigmentation, and Telangiectatic Nevi of the Lower Limbs: A Novel Variant of the Phacomatosis ComplexCASTORI, Marco; SCARCIOLLA, Oronzo; MORLINO, Silvia et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 2, pp 445-449, issn 1552-4825, 5 p.Article

Reassessment of Oral Frenula in Ehlers―Danlos Syndrome: A Study of 32 Patients With the Hypermobility TypeCELLETTI, Claudia; CASTORI, Marco; LA TORRE, Giuseppe et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3157-3159, issn 1552-4825, 3 p.Article

Gait strategy in patients with Ehlers-Danlos syndrome hypermobility type: A kinematic and kinetic evaluation using 3D gait analysisGALLI, Manuela; CIMOLIN, Veronica; RIGOLDI, Chiara et al.Research in developmental disabilities (Print). 2011, Vol 32, Num 5, pp 1663-1668, issn 0891-4222, 6 p.Article

Palmoplantar keratoderma in keratosis follicularis spinulosa decalvansANTONIETTA, Maria; CASTORI, Marco; MASALA, Maria Vittoria et al.EJD. European journal of dermatology. 2010, Vol 20, Num 6, pp 850-852, issn 1167-1122, 3 p.Article

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