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Diseases (Basel, Switzerland)
|
June 25, 2025
Germline Non-CDKN2A Variants in Melanoma and Associated Hereditary Cancer Syndromes
Chiara Anna Fiasconaro, Alice Carbone, Silvia Giordano, et al.
Tumori
|
July 5, 2003
Breast MRI screening in patients with increased familial and/or genetic risk for breast cancer: a preliminary experience
Giovanna Trecate, Daniele Vergnaghi, Silvana Bergonzi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
May 11, 2002
Lack of SYT-SSX fusion transcripts in malignant peripheral nerve sheath tumors on RT-PCR analysis of 34 archival cases
Elena Tamborini, Viviana Agus, Federica Perrone, et al.
Journal of Clinical Medicine
|
July 9, 2022
Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General Population
Valentina Elisabetta Bounous, Elisabetta Robba, Stefania Perotto, et al.
Surgery
|
April 28, 2005
The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case
Antonella Aiello, Katia Cioni, Morena Gobbo, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 4, 2024
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit
Martina Tetti, Jacopo Burrello, Marguerite Hureaux, et al.
Hypertension (Dallas, Tex. : 1979)
|
March 3, 2020
Prevalence of Hypokalemia and Primary Aldosteronism in 5100 Patients Referred to a Tertiary Hypertension Unit
Jacopo Burrello, Silvia Monticone, Isabel Losano, et al.
Medicina (Kaunas, Lithuania)
|
July 10, 2019
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism
Laura Cristina Gironi, Enrico Colombo, Alfredo Brusco, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin
Iolanda Borelli, Marco A Barberis, Francesca Spina, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia
|
July 13, 2017
[Hyperuricemia and gene mutations: a case report]
Fabio Tattoli, Daniela Falconi, Ornella De Prisco, et al.
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Search research articles
Search
Showing results (21-30 of 96) with videos related to
Sort By:
Page
of 10
Diseases (Basel, Switzerland)
|
June 25, 2025
Germline Non-CDKN2A Variants in Melanoma and Associated Hereditary Cancer Syndromes
Chiara Anna Fiasconaro, Alice Carbone, Silvia Giordano, et al.
Tumori
|
July 5, 2003
Breast MRI screening in patients with increased familial and/or genetic risk for breast cancer: a preliminary experience
Giovanna Trecate, Daniele Vergnaghi, Silvana Bergonzi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
May 11, 2002
Lack of SYT-SSX fusion transcripts in malignant peripheral nerve sheath tumors on RT-PCR analysis of 34 archival cases
Elena Tamborini, Viviana Agus, Federica Perrone, et al.
Journal of Clinical Medicine
|
July 9, 2022
Gynecological Cancers in Lynch Syndrome: A Comparison of the Histological Features with Sporadic Cases of the General Population
Valentina Elisabetta Bounous, Elisabetta Robba, Stefania Perotto, et al.
Surgery
|
April 28, 2005
The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case
Antonella Aiello, Katia Cioni, Morena Gobbo, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 4, 2024
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit
Martina Tetti, Jacopo Burrello, Marguerite Hureaux, et al.
Hypertension (Dallas, Tex. : 1979)
|
March 3, 2020
Prevalence of Hypokalemia and Primary Aldosteronism in 5100 Patients Referred to a Tertiary Hypertension Unit
Jacopo Burrello, Silvia Monticone, Isabel Losano, et al.
Medicina (Kaunas, Lithuania)
|
July 10, 2019
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism
Laura Cristina Gironi, Enrico Colombo, Alfredo Brusco, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin
Iolanda Borelli, Marco A Barberis, Francesca Spina, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia
|
July 13, 2017
[Hyperuricemia and gene mutations: a case report]
Fabio Tattoli, Daniela Falconi, Ornella De Prisco, et al.
Page
of 10