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Movement Disorders : Official Journal of the Movement Disorder Society
|
October 5, 2007
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements
Oronzo Scarciolla, Francesco Brancati, Enza Maria Valente, et al.
International Journal of Audiology
|
September 28, 2012
Audiological and radiological characteristics of a family with T961G mitochondrial mutation
Rosaria Turchetta, Filippo Mazzei, Tiziana Celani, et al.
Inflammatory Bowel Diseases
|
May 4, 2006
Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study
Alessandro Ferraris, Barbara Torres, Daniela Knafelz, et al.
Polymers
|
December 1, 2020
Validation of a Simulation Methodology for Thermoplastic and Thermosetting Composite Materials Considering the Effect of Forming Process on the Structural Performance
Lorenzo Sisca, Patrizio Tiziano Locatelli Quacchia, Alessandro Messana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 17, 2013
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria
Miryam Carecchio, Monia Magliozzi, Massimiliano Copetti, et al.
Orphanet Journal of Rare Diseases
|
June 10, 2011
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients
Marilena Briguglio, Lorenzo Pinelli, Lucio Giordano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 6, 2009
Olfactory dysfunction in Parkinsonism caused by PINK1 mutations
Alessandro Ferraris, Tamara Ialongo, Giulio Cesare Passali, et al.
RMD Open
|
November 8, 2018
Ehlers-Danlos syndromes: state of the art on clinical practice guidelines
Alberto Sulli, Rosaria Talarico, Carlo Alberto Scirè, et al.
European Journal of Human Genetics : EJHG
|
December 18, 2022
Two unrelated cases with biallelic CHEK2 variants:a novel condition with constitutional chromosomal instability?
Irene Bottillo, Emanuele Savino, Silvia Majore, et al.
Prenatal Diagnosis
|
May 4, 2022
Discordant cfDNA-NIPT result unraveling a trisomy 12 chronic lymphocytic leukemia in a 37 years old pregnant woman
Niccolò Di Giosaffatte, Irene Bottillo, Luigi Laino, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 5, 2007
Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements
Oronzo Scarciolla, Francesco Brancati, Enza Maria Valente, et al.
International Journal of Audiology
|
September 28, 2012
Audiological and radiological characteristics of a family with T961G mitochondrial mutation
Rosaria Turchetta, Filippo Mazzei, Tiziana Celani, et al.
Inflammatory Bowel Diseases
|
May 4, 2006
Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study
Alessandro Ferraris, Barbara Torres, Daniela Knafelz, et al.
Polymers
|
December 1, 2020
Validation of a Simulation Methodology for Thermoplastic and Thermosetting Composite Materials Considering the Effect of Forming Process on the Structural Performance
Lorenzo Sisca, Patrizio Tiziano Locatelli Quacchia, Alessandro Messana, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 17, 2013
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria
Miryam Carecchio, Monia Magliozzi, Massimiliano Copetti, et al.
Orphanet Journal of Rare Diseases
|
June 10, 2011
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients
Marilena Briguglio, Lorenzo Pinelli, Lucio Giordano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 6, 2009
Olfactory dysfunction in Parkinsonism caused by PINK1 mutations
Alessandro Ferraris, Tamara Ialongo, Giulio Cesare Passali, et al.
RMD Open
|
November 8, 2018
Ehlers-Danlos syndromes: state of the art on clinical practice guidelines
Alberto Sulli, Rosaria Talarico, Carlo Alberto Scirè, et al.
European Journal of Human Genetics : EJHG
|
December 18, 2022
Two unrelated cases with biallelic CHEK2 variants:a novel condition with constitutional chromosomal instability?
Irene Bottillo, Emanuele Savino, Silvia Majore, et al.
Prenatal Diagnosis
|
May 4, 2022
Discordant cfDNA-NIPT result unraveling a trisomy 12 chronic lymphocytic leukemia in a 37 years old pregnant woman
Niccolò Di Giosaffatte, Irene Bottillo, Luigi Laino, et al.
Page
of 6