D Z Loesch|M Lafranchi|C Ruffolo - JoVE Visualize

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American Journal of Medical Genetics|June 1, 1987

Phenotypic variation in male-transmitted fragile X: genetic inferencesD Z Loesch, D A Hay, G R Sutherland, et al.

Journal of Chemotherapy (Florence, Italy)|April 9, 2002

Antibiotic prophylaxis in clean surgery: breast surgery and hernia repairD F D'Amico, P Parimbelli, C Ruffolo

Public Health Reports (Washington, D.C. : 1974)|May 25, 2023

Building a Community-Academic Partnership to Expand Workforce Development in Underserved, High-Need/High-Demand AreasMary C Ruffolo, Daicia Price, Andrea Smith

American Journal of Human Genetics|November 1, 1993

Genotype-phenotype relationships in fragile X syndrome: a family studyD Z Loesch, R Huggins, D A Hay, et al.

Clinical Genetics|April 12, 2011

Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 geneD Z Loesch, S Sherwell, G Kinsella, et al.

Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|August 14, 2009

A systematic review on advancement flaps for rectovaginal fistula in Crohn's disease: transrectal vs transvaginal approachC Ruffolo, M Scarpa, N Bassi, et al.

Journal of Medical Genetics|December 7, 2007

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.

Updates in Surgery|January 19, 2017

Should we routinely use DEBTACE for unresectable HCC? cTACE versus DEBTACE: a single-center survival analysisM Massani, T Stecca, C Ruffolo, et al.

American Journal of Medical Genetics|February 24, 2001

Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary studyE L Gould, D Z Loesch, M J Martin, et al.

American Journal of Medical Genetics. Part A|September 2, 2003

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysisD Z Loesch, R M Huggins, Q M Bui, et al.

Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:

Pageof 10

American Journal of Medical Genetics|June 1, 1987

Phenotypic variation in male-transmitted fragile X: genetic inferencesD Z Loesch, D A Hay, G R Sutherland, et al.

Journal of Chemotherapy (Florence, Italy)|April 9, 2002

Antibiotic prophylaxis in clean surgery: breast surgery and hernia repairD F D'Amico, P Parimbelli, C Ruffolo

Public Health Reports (Washington, D.C. : 1974)|May 25, 2023

Building a Community-Academic Partnership to Expand Workforce Development in Underserved, High-Need/High-Demand AreasMary C Ruffolo, Daicia Price, Andrea Smith

American Journal of Human Genetics|November 1, 1993

Genotype-phenotype relationships in fragile X syndrome: a family studyD Z Loesch, R Huggins, D A Hay, et al.

Clinical Genetics|April 12, 2011

Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 geneD Z Loesch, S Sherwell, G Kinsella, et al.

Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|August 14, 2009

A systematic review on advancement flaps for rectovaginal fistula in Crohn's disease: transrectal vs transvaginal approachC Ruffolo, M Scarpa, N Bassi, et al.

Journal of Medical Genetics|December 7, 2007

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.

Updates in Surgery|January 19, 2017

Should we routinely use DEBTACE for unresectable HCC? cTACE versus DEBTACE: a single-center survival analysisM Massani, T Stecca, C Ruffolo, et al.

American Journal of Medical Genetics|February 24, 2001

Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary studyE L Gould, D Z Loesch, M J Martin, et al.

American Journal of Medical Genetics. Part A|September 2, 2003

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysisD Z Loesch, R M Huggins, Q M Bui, et al.

Pageof 10