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Friedrich Stock

Showing results (21-30 of 31) with videos related to

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Frontiers in Psychiatry|May 24, 2019
Schizophrenia and Hereditary Polyneuropathy: <i>PMP22</i> Deletion as a Common Pathophysiological Link?Dominique Endres, Simon J Maier, Christiane Ziegler, et al.
World Journal of Urology|August 20, 2022
Ultrasound-based "CEUS-Bosniak"classification for cystic renal lesions: an 8-year clinical experienceElena Herms, Gregor Weirich, Tobias Maurer, et al.
Frontiers in Immunology|April 6, 2019
New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the <i>MT-ND4</i> Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2Dominique Endres, Patrick Süß, Simon J Maier, et al.
The Journal of Investigative Dermatology|April 4, 2013
Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain lengthKatja-Martina Eckl, Rotem Tidhar, Holger Thiele, et al.
Diagnostics (Basel, Switzerland)|February 10, 2024
Postmortem Minimally Invasive Autopsy in Critically Ill COVID-19 Patients at the Bedside: A Proof-of-Concept Study at the ICUTobias Lahmer, Gregor Weirich, Stefan Porubsky, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|December 11, 2020
EFSUMB 2020 Proposal for a Contrast-Enhanced Ultrasound-Adapted Bosniak Cyst Categorization - Position StatementVito Cantisani, Michele Bertolotto, Dirk-André Clevert, et al.
Journal of Medical Genetics|April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumChristine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
JCO Precision Oncology|September 11, 2020
Personalized Clinical Decision Making Through Implementation of a Molecular Tumor Board: A German Single-Center ExperienceRouven Hoefflin, Anna-Lena Geißler, Ralph Fritsch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Frontiers in Psychiatry|May 24, 2019
Schizophrenia and Hereditary Polyneuropathy: <i>PMP22</i> Deletion as a Common Pathophysiological Link?Dominique Endres, Simon J Maier, Christiane Ziegler, et al.
World Journal of Urology|August 20, 2022
Ultrasound-based "CEUS-Bosniak"classification for cystic renal lesions: an 8-year clinical experienceElena Herms, Gregor Weirich, Tobias Maurer, et al.
Frontiers in Immunology|April 6, 2019
New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the <i>MT-ND4</i> Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2Dominique Endres, Patrick Süß, Simon J Maier, et al.
The Journal of Investigative Dermatology|April 4, 2013
Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain lengthKatja-Martina Eckl, Rotem Tidhar, Holger Thiele, et al.
Diagnostics (Basel, Switzerland)|February 10, 2024
Postmortem Minimally Invasive Autopsy in Critically Ill COVID-19 Patients at the Bedside: A Proof-of-Concept Study at the ICUTobias Lahmer, Gregor Weirich, Stefan Porubsky, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|December 11, 2020
EFSUMB 2020 Proposal for a Contrast-Enhanced Ultrasound-Adapted Bosniak Cyst Categorization - Position StatementVito Cantisani, Michele Bertolotto, Dirk-André Clevert, et al.
Journal of Medical Genetics|April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumChristine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
JCO Precision Oncology|September 11, 2020
Personalized Clinical Decision Making Through Implementation of a Molecular Tumor Board: A German Single-Center ExperienceRouven Hoefflin, Anna-Lena Geißler, Ralph Fritsch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 4