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Michele Callea

Showing results (1-10 of 42) with videos related to

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Children (Basel, Switzerland)|May 28, 2022
Pathophysiology, Management and Quality of Life in Atopic Dermatitis and Psoriasis-A Challenge for Patients and Their FamiliesMichele Callea
Archivos Argentinos De Pediatria|November 21, 2018
Main genetic entities associated with supernumerary teethFrancisco Cammarata-Scalisi, Andrea Avendaño, Michele Callea
BMJ Case Reports|April 12, 2013
A new biological approach to guided bone and tissue regenerationMarco Montanari, Michele Callea, Izzet Yavuz, et al.
BMJ Case Reports|June 26, 2012
Oral rehabilitation of children with ectodermal dysplasiaMarco Montanari, Michele Callea, Filippo Battelli, et al.
Journal of Clinical and Experimental Dentistry|October 6, 2023
Extensive dental caries and periodontal disease in a child with GATA2 deficiencyFilippo Consonni, Eleonora Gambineri, Marinella Veltroni, et al.
BMJ Case Reports|December 11, 2012
A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 geneMichele Callea, Fabiana Fattori, Izzet Yavuz, et al.
Hormones (Athens, Greece)|June 3, 2018
5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A reviewAndrea Avendaño, Irene Paradisi, Francisco Cammarata-Scalisi, et al.
Archivos Argentinos De Pediatria|November 24, 2015
[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]Michele Callea, Izzet Yavuz, Gabriella Clarich, et al.
Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
X-linked reticulate pigmentary disorder with systemic manifestations: a new family and review of the literatureLidia Pezzani, Michela Brena, Michele Callea, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Children (Basel, Switzerland)|May 28, 2022
Pathophysiology, Management and Quality of Life in Atopic Dermatitis and Psoriasis-A Challenge for Patients and Their FamiliesMichele Callea
Archivos Argentinos De Pediatria|November 21, 2018
Main genetic entities associated with supernumerary teethFrancisco Cammarata-Scalisi, Andrea Avendaño, Michele Callea
BMJ Case Reports|April 12, 2013
A new biological approach to guided bone and tissue regenerationMarco Montanari, Michele Callea, Izzet Yavuz, et al.
BMJ Case Reports|June 26, 2012
Oral rehabilitation of children with ectodermal dysplasiaMarco Montanari, Michele Callea, Filippo Battelli, et al.
Journal of Clinical and Experimental Dentistry|October 6, 2023
Extensive dental caries and periodontal disease in a child with GATA2 deficiencyFilippo Consonni, Eleonora Gambineri, Marinella Veltroni, et al.
BMJ Case Reports|December 11, 2012
A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 geneMichele Callea, Fabiana Fattori, Izzet Yavuz, et al.
Hormones (Athens, Greece)|June 3, 2018
5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A reviewAndrea Avendaño, Irene Paradisi, Francisco Cammarata-Scalisi, et al.
Archivos Argentinos De Pediatria|November 24, 2015
[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]Michele Callea, Izzet Yavuz, Gabriella Clarich, et al.
Children (Basel, Switzerland)|May 16, 2023
Challenges in Communicating a Genetic DiagnosisFrancisco Cammarata-Scalisi, Colin Eric Willoughby, Vito Romano, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
X-linked reticulate pigmentary disorder with systemic manifestations: a new family and review of the literatureLidia Pezzani, Michela Brena, Michele Callea, et al.
Pageof 5