F Tassone|P J Hagerman - JoVE Visualize

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Parkinsonism & Related Disorders|August 13, 2010

FMR1 gene expansion and scans without evidence of dopaminergic deficits in parkinsonism patientsD A Hall, D Jennings, J Seibyl, et al.

Clinical Genetics|April 7, 2005

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyondD Z Loesch, A Churchyard, P Brotchie, et al.

American Journal of Human Genetics|April 6, 2004

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutationR J Hagerman, B R Leavitt, F Farzin, et al.

Neuroepidemiology|February 24, 2006

Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.

Giornale Italiano Di Cardiologia|April 1, 1985

[A new dual-chamber pacemaker with an automatic antitachycardia system in the treatment of the bradycardia-tachycardia syndrome]E Adornato, R M Polimeni, P Monea, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|July 14, 2012

Tacrolimus 0.1% ointment in nail psoriasis: a randomized controlled open-label studyC De Simone, A Maiorino, F Tassone, et al.

RMD Open|March 2, 2023

Antibody response to the COVID-19 ChAdOx1nCov-19 and BNT162b vaccines after temporary suspension of DMARD therapy in immune-mediated inflammatory disease: an extension study (RESCUE 2)Ai Phuong Tran, D F Tassone, N S Ding, et al.

American Journal of Medical Genetics. Supplement|January 1, 1990

Potential gene sequence isolation and regional mapping in human chromosome 21C Brahe, F Tassone, A Millington-Ward, et al.

Gene|May 23, 1998

Analysis of pufferfish homologues of the AT-rich human APP geneL Villard, F Tassone, T Crnogorac-Jurcević, et al.

Annals of Human Genetics|October 1, 1987

Family and population studies of SAHH and ADA polymorphisms. A possible pitfall in the ascertainment of SAHH electrophoretic phenotypesR Scozzari, D Sellitto, F Tassone, et al.

Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:

Pageof 16

Parkinsonism & Related Disorders|August 13, 2010

FMR1 gene expansion and scans without evidence of dopaminergic deficits in parkinsonism patientsD A Hall, D Jennings, J Seibyl, et al.

Clinical Genetics|April 7, 2005

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyondD Z Loesch, A Churchyard, P Brotchie, et al.

American Journal of Human Genetics|April 6, 2004

Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutationR J Hagerman, B R Leavitt, F Farzin, et al.

Neuroepidemiology|February 24, 2006

Prevalence of FMR1 repeat expansions in movement disorders. A systematic reviewD A Hall, R J Hagerman, P J Hagerman, et al.

Giornale Italiano Di Cardiologia|April 1, 1985

[A new dual-chamber pacemaker with an automatic antitachycardia system in the treatment of the bradycardia-tachycardia syndrome]E Adornato, R M Polimeni, P Monea, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|July 14, 2012

Tacrolimus 0.1% ointment in nail psoriasis: a randomized controlled open-label studyC De Simone, A Maiorino, F Tassone, et al.

RMD Open|March 2, 2023

Antibody response to the COVID-19 ChAdOx1nCov-19 and BNT162b vaccines after temporary suspension of DMARD therapy in immune-mediated inflammatory disease: an extension study (RESCUE 2)Ai Phuong Tran, D F Tassone, N S Ding, et al.

American Journal of Medical Genetics. Supplement|January 1, 1990

Potential gene sequence isolation and regional mapping in human chromosome 21C Brahe, F Tassone, A Millington-Ward, et al.

Gene|May 23, 1998

Analysis of pufferfish homologues of the AT-rich human APP geneL Villard, F Tassone, T Crnogorac-Jurcević, et al.

Annals of Human Genetics|October 1, 1987

Family and population studies of SAHH and ADA polymorphisms. A possible pitfall in the ascertainment of SAHH electrophoretic phenotypesR Scozzari, D Sellitto, F Tassone, et al.

Pageof 16