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D Franceschini

Showing results (21-30 of 69) with videos related to

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Genetic Counseling (Geneva, Switzerland)|May 23, 2002
A mentally retarded female with distinct facial dysmorphism, joint laxity, clinodactyly and abnormal dermatoglyphicsP Franceschini, A Guala, D Besana, et al.
Clinical Dysmorphology|July 1, 1994
Rigid mask-like face, ear anomalies, deafness, preaxial polydactyly and toe malformations in a patient with normal intelligence: a new entity?P Franceschini, M P Vardeu, A Guala, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2001
Melatonin protects against 6-OHDA-induced neurotoxicity in rats: a role for mitochondrial complex I activityF Dabbeni-Sala, Di Santo S, D Franceschini, et al.
American Journal of Medical Genetics|March 1, 1996
Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18P Franceschini, A Guala, P Camerano, et al.
British Journal of Anaesthesia|February 5, 2018
Prevention of arterial hypotension after spinal anaesthesia using vena cava ultrasound to guide fluid managementS Ceruti, L Anselmi, B Minotti, et al.
American Journal of Medical Genetics|November 20, 1995
Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrumP Franceschini, A Guala, M P Vardeu, et al.
American Journal of Medical Genetics|December 1, 1992
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeP Franceschini, M P Vardeu, L Dalforno, et al.
American Journal of Medical Genetics|September 1, 1993
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndromeP Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the diseaseP Franceschini, M P Vardeu, F Signorile, et al.
American Journal of Medical Genetics|August 17, 1999
Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and reviewP Franceschini, D Licata, G Di Cara, et al.
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
A mentally retarded female with distinct facial dysmorphism, joint laxity, clinodactyly and abnormal dermatoglyphicsP Franceschini, A Guala, D Besana, et al.
Clinical Dysmorphology|July 1, 1994
Rigid mask-like face, ear anomalies, deafness, preaxial polydactyly and toe malformations in a patient with normal intelligence: a new entity?P Franceschini, M P Vardeu, A Guala, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2001
Melatonin protects against 6-OHDA-induced neurotoxicity in rats: a role for mitochondrial complex I activityF Dabbeni-Sala, Di Santo S, D Franceschini, et al.
American Journal of Medical Genetics|March 1, 1996
Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18P Franceschini, A Guala, P Camerano, et al.
British Journal of Anaesthesia|February 5, 2018
Prevention of arterial hypotension after spinal anaesthesia using vena cava ultrasound to guide fluid managementS Ceruti, L Anselmi, B Minotti, et al.
American Journal of Medical Genetics|November 20, 1995
Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrumP Franceschini, A Guala, M P Vardeu, et al.
American Journal of Medical Genetics|December 1, 1992
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeP Franceschini, M P Vardeu, L Dalforno, et al.
American Journal of Medical Genetics|September 1, 1993
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndromeP Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the diseaseP Franceschini, M P Vardeu, F Signorile, et al.
American Journal of Medical Genetics|August 17, 1999
Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and reviewP Franceschini, D Licata, G Di Cara, et al.
Pageof 7