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Barbara Kocsis

Showing results (1-10 of 8) with videos related to

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Psychiatric Services (Washington, D.C.)|January 18, 2019
Ethical Considerations Regarding Internet Searches for Patient InformationCharles C Dike, Philip Candilis, Barbara Kocsis, et al.
Archives of Dermatological Research|September 18, 2015
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutationEdina Nemes, Katalin Farkas, Barbara Kocsis-Deák, et al.
Orvosi Hetilap|September 8, 2019
[Genetic testing of thyroid nodules using a gene panel developed on a new generation sequencing platform]Barbara Kocsis-Deák, Bernadett Balla, Kristóf Árvai, et al.
The Journal of Steroid Biochemistry and Molecular Biology|January 28, 2019
Long-term selective estrogen receptor-beta agonist treatment modulates gene expression in bone and bone marrow of ovariectomized ratsBernadett Balla, Miklós Sárvári, János P Kósa, et al.
Pathology Oncology Research : POR|November 24, 2019
Targeted Mutational Profiling and a Powerful Risk Score as Additional Tools for the Diagnosis of Papillary Thyroid CancerBarbara Kocsis-Deák, Kristóf Árvai, Bernadett Balla, et al.
Placenta|February 27, 2019
Increased placental expression of Placental Protein 5 (PP5) / Tissue Factor Pathway Inhibitor-2 (TFPI-2) in women with preeclampsia and HELLP syndrome: Relevance to impaired trophoblast invasion?Katalin Karaszi, Szilvia Szabo, Kata Juhasz, et al.
BMC Endocrine Disorders|January 26, 2023
Comparison of surgical strategies in the treatment of low-risk differentiated thyroid cancerAndrás Kiss, Balázs Szili, Bence Bakos, et al.
BMC Genetics|February 11, 2016
The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the geneKatalin Farkas, Barbara Kocsis Deák, Laura Cubells Sánchez, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Psychiatric Services (Washington, D.C.)|January 18, 2019
Ethical Considerations Regarding Internet Searches for Patient InformationCharles C Dike, Philip Candilis, Barbara Kocsis, et al.
Archives of Dermatological Research|September 18, 2015
Phenotypical diversity of patients with LEOPARD syndrome carrying the worldwide recurrent p.Tyr279Cys PTPN11 mutationEdina Nemes, Katalin Farkas, Barbara Kocsis-Deák, et al.
Orvosi Hetilap|September 8, 2019
[Genetic testing of thyroid nodules using a gene panel developed on a new generation sequencing platform]Barbara Kocsis-Deák, Bernadett Balla, Kristóf Árvai, et al.
The Journal of Steroid Biochemistry and Molecular Biology|January 28, 2019
Long-term selective estrogen receptor-beta agonist treatment modulates gene expression in bone and bone marrow of ovariectomized ratsBernadett Balla, Miklós Sárvári, János P Kósa, et al.
Pathology Oncology Research : POR|November 24, 2019
Targeted Mutational Profiling and a Powerful Risk Score as Additional Tools for the Diagnosis of Papillary Thyroid CancerBarbara Kocsis-Deák, Kristóf Árvai, Bernadett Balla, et al.
Placenta|February 27, 2019
Increased placental expression of Placental Protein 5 (PP5) / Tissue Factor Pathway Inhibitor-2 (TFPI-2) in women with preeclampsia and HELLP syndrome: Relevance to impaired trophoblast invasion?Katalin Karaszi, Szilvia Szabo, Kata Juhasz, et al.
BMC Endocrine Disorders|January 26, 2023
Comparison of surgical strategies in the treatment of low-risk differentiated thyroid cancerAndrás Kiss, Balázs Szili, Bence Bakos, et al.
BMC Genetics|February 11, 2016
The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the geneKatalin Farkas, Barbara Kocsis Deák, Laura Cubells Sánchez, et al.
Pageof 1