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Mostrati risultati da 1 a 20 di 113
Titolo Data di pubblicazione Autore(i) File
Esophageal atresia with distal tracheoesophageal fistula in a patient with fronto-metaphyseal dysplasia. 1997 Franceschini, P; Guala, A; Licata, D; Franceschini, D; Signorile, F; DI CARA, Giuseppe
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome 1998 Franceschini, P; Licata, D; Guala, A; DI CARA, Giuseppe; Signorile, F; Franceschini, D; Genitori, L; Restagno, G.
Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and review. 1999 Franceschini, P; Licata, D; DI CARA, Giuseppe; Guala, A; Bianchi, M; Ingrosso, G; Franceschini, D.
Macrocephaly-Cutis marmorata telangiectatica congenita without cutis marmorata? 2000 Franceschini, P; Licata, D; DI CARA, Giuseppe; Guala, A; Franceschini, D; Genitori, L.
Radioulnar synostosis and XYY syndrome. 2000 Franceschini, P; Licata, D; Guala, A; DI CARA, Giuseppe; Franceschini, D.
Arterial tortuosity syndrome. 2000 Franceschini, P; Guala, A; Licata, D; DI CARA, Giuseppe; Franceschini, D.
Prenatal diagnosis of kyphomelic dysplasia. 2001 Guala, A; Biroli, E; Bassini, P; Botta, G; Licata, D; DI CARA, Giuseppe; Franceschini, D; Franceschini, P.
Peculiar facial appearance and generalized brachydactyly in a patient with congenital onychodysplasia of the index fingers (Iso-Kikuchi syndrome). 2001 Franceschini, P; Licata, D; Guala, A; DI CARA, Giuseppe; Franceschini, D.
Prenatal diagnosis of Nonne-Milroy lymphedema. 2001 Franceschini, P; Licata, D; Rapello, G; Guala, A; DI CARA, Giuseppe; Franceschini, D.
Filippisyndrome: a specific MCA/MR complex within the spectrum of so called"craniodigital syndromes". Report of an additional patient with a peculiar mppand review of the literature. 2002 Franceschini, P; Licata, D; Guala, A; DI CARA, Giuseppe; Franceschini, D.
Amentally retarded female with distinct facial dysmorphism, joint laxity,clinodactyly and abnormal dermatoglyphics. 2002 Franceschini, P; Guala, A; Besana, D; Licata, D; DI CARA, Giuseppe; Franceschini, D.
Poland sequence and hyperhomocyst(e)inaemia. 2002 Franceschini, P; Licata, D; Guala, A; DI CARA, Giuseppe; Franceschini, D.
Gershoni-Baruch syndrome: report of a new family confirmingautosomal recessive inheritance. 2003 Franceschini, P; Guala, A; Licata, D; Botta, G; Flora, F; Angeli, G; DI CARA, Giuseppe; Franceschini, D.
A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries? 2003 Franceschini, P; Guala, A; Licata, D; DI CARA, Giuseppe; Franceschini, D.
Measurement of nasal IgE in an epidemiological study: assessment of its diagnostic value in respiratory allergy. 2004 Marcucci, F; Passalacqua, G; Canonica, Gw; Frati, F; Salvatori, S; DI CARA, Giuseppe; Bernini, M; Barbato, A; Mastrandrea, F; Sensi, L. G.
Patterson-Lowry rhizomelic dysplasia: report of two new patients. 2004 Franceschini, P; Licata, D; Guala, A; Ingrosso, G; DI CARA, Giuseppe; Franceschini, D.
Three-year follow-up of clinical and inflammation parameters in children monosensitized to mites undergoing sub-lingual immunotherapy. 2005 Marcucci, Francesco; Sensi, Laura Giovanna; DI CARA, Giuseppe; Salvatori, S; Bernini, M; Pecora, S; Burastero, Se
Dose dependence of immunological response to sublingual immunotherapy. 2005 Marcucci, Francesco; Sensi, Laura Giovanna; DI CARA, Giuseppe; Incorvaia, C; Frati, F.
Preliminary results about macrogol 4000 for treatment of constipation in children XII Congresso Nazionale SIGENP 2005 2005 Bertozzi, M.; Balossini, F.; Prestipino, M.; DI CARA, Giuseppe; Brunero, M.; Vicchio, N.; Matteotti, C.; Appignani, Antonino
Evaluation of food-pollen cross-reactivity by nose-mouth cross-challenge in pollinosis with oral allergy syndrome. 2005 Marcucci, F; Frati, F; Sensi, L; DI CARA, Giuseppe; Novembre, E; Bernardini, R; Canonica, Gw; Passalacqua, G.
Mostrati risultati da 1 a 20 di 113
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