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American Journal of Medical Genetics. Part A
|
March 2, 2019
Cardiac valvular Ehlers-Danlos syndrome is a well-defined condition due to recessive null variants in COL1A2
Vito Guarnieri, Silvia Morlino, Giuseppe Di Stolfo, et al.
Research in Developmental Disabilities
|
March 23, 2011
Gait strategy in patients with Ehlers-Danlos syndrome hypermobility type: a kinematic and kinetic evaluation using 3D gait analysis
Manuela Galli, Veronica Cimolin, Chiara Rigoldi, et al.
Journal of Dermatological Science
|
April 5, 2008
Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa
Marco Castori, Giovanna Floriddia, Elisa Pisaneschi, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2006
Antenatal presentation of the oculo-auriculo-vertebral spectrum (OAVS)
Marco Castori, Francesco Brancati, Rosanna Rinaldi, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
Review of clinical and molecular variability in autosomal recessive cutis laxa 2A
Silvia Morlino, Grazia Nardella, Stefano Castellana, et al.
Genes
|
May 4, 2026
A 350 kb <i>NEXMIF</i> Microdeletion Identified by Chromosomal Microarray in an Adult Patient with Jeavons Syndrome
Mario Benvenuto, Umberto Costantino, Pietro Palumbo, et al.
Arthritis Care & Research
|
January 18, 2011
Evaluation of balance and improvement of proprioception by repetitive muscle vibration in a 15-year-old girl with joint hypermobility syndrome
Claudia Celletti, Marco Castori, Manuela Galli, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace
|
May 22, 2020
A new insight on postural tachycardia syndrome in 102 adults with hypermobile Ehlers-Danlos Syndrome/hypermobility spectrum disorder
Claudia Celletti, Beatrice Borsellino, Marco Castori, et al.
Clinical Genetics
|
October 11, 2019
Application of the 2017 criteria for vascular Ehlers-Danlos syndrome in 50 patients ascertained according to the Villefranche nosology
Marco Ritelli, Chiara Rovati, Marina Venturini, et al.
American Journal of Medical Genetics. Part A
|
January 17, 2012
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex"
Marco Castori, Oronzo Scarciolla, Silvia Morlino, et al.
Page
of 24
Search research articles
Search
Showing results (71-80 of 239) with videos related to
Sort By:
Page
of 24
American Journal of Medical Genetics. Part A
|
March 2, 2019
Cardiac valvular Ehlers-Danlos syndrome is a well-defined condition due to recessive null variants in COL1A2
Vito Guarnieri, Silvia Morlino, Giuseppe Di Stolfo, et al.
Research in Developmental Disabilities
|
March 23, 2011
Gait strategy in patients with Ehlers-Danlos syndrome hypermobility type: a kinematic and kinetic evaluation using 3D gait analysis
Manuela Galli, Veronica Cimolin, Chiara Rigoldi, et al.
Journal of Dermatological Science
|
April 5, 2008
Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa
Marco Castori, Giovanna Floriddia, Elisa Pisaneschi, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2006
Antenatal presentation of the oculo-auriculo-vertebral spectrum (OAVS)
Marco Castori, Francesco Brancati, Rosanna Rinaldi, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
Review of clinical and molecular variability in autosomal recessive cutis laxa 2A
Silvia Morlino, Grazia Nardella, Stefano Castellana, et al.
Genes
|
May 4, 2026
A 350 kb <i>NEXMIF</i> Microdeletion Identified by Chromosomal Microarray in an Adult Patient with Jeavons Syndrome
Mario Benvenuto, Umberto Costantino, Pietro Palumbo, et al.
Arthritis Care & Research
|
January 18, 2011
Evaluation of balance and improvement of proprioception by repetitive muscle vibration in a 15-year-old girl with joint hypermobility syndrome
Claudia Celletti, Marco Castori, Manuela Galli, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace
|
May 22, 2020
A new insight on postural tachycardia syndrome in 102 adults with hypermobile Ehlers-Danlos Syndrome/hypermobility spectrum disorder
Claudia Celletti, Beatrice Borsellino, Marco Castori, et al.
Clinical Genetics
|
October 11, 2019
Application of the 2017 criteria for vascular Ehlers-Danlos syndrome in 50 patients ascertained according to the Villefranche nosology
Marco Ritelli, Chiara Rovati, Marina Venturini, et al.
American Journal of Medical Genetics. Part A
|
January 17, 2012
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex"
Marco Castori, Oronzo Scarciolla, Silvia Morlino, et al.
Page
of 24