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Behavioral Medicine (Washington, D.C.)
|
October 29, 2005
Surveillance behavior and prophylactic surgery after predictive testing for hereditary breast/ovarian cancer
Erna Claes, Gerry Evers-Kiebooms, Marleen Decruyenaere, et al.
Pediatric Dermatology
|
February 11, 2026
Novel Identical Likely Pathogenic ACTB Variant in Congenital Smooth Muscle Hamartoma: A Report of Two Pediatric Cases
Caroline Colmant, Eric Legius, Ifigenia Spanoudi-Kitrimi, et al.
Revue Medicale Suisse
|
March 26, 2026
[Pigmentary mosaicism: a literature review]
Selin Yener, Jean-Marc Good, Daniel Hohl, et al.
Neurology
|
November 1, 2015
Behavioral and cognitive outcomes for clinical trials in children with neurofibromatosis type 1
Thijs van der Vaart, André B Rietman, Ellen Plasschaert, et al.
European Journal of Endocrinology
|
September 15, 2023
Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families
Axelle Vuylsteke, Laurens Hannes, Hilde Brems, et al.
Nature Communications
|
February 22, 2023
SREBP modulates the NADP<sup>+</sup>/NADPH cycle to control night sleep in Drosophila
Vittoria Mariano, Alexandros K Kanellopoulos, Giuseppe Aiello, et al.
Pediatric Blood & Cancer
|
August 4, 2005
Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation
Christophe F Chantrain, Priscilla Jijon, Thomas De Raedt, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
December 4, 2009
Does paclitaxel-carboplatin chemotherapy in a dose-dense regimen enhance survival of BRCA-related ovarian cancer patients?
Karin Leunen, Isabelle Cadron, Toon Van Gorp, et al.
Surgical Neurology International
|
December 17, 2013
What the neurosurgeon should know about hemangioblastoma, both sporadic and in Von Hippel-Lindau disease: A literature review
Sven Bamps, Frank Van Calenbergh, Steven De Vleeschouwer, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2002
Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD)
Geneviève Michils, Sabine Tejpar, Jean-Pierre Fryns, et al.
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of 17
Search research articles
Search
Showing results (31-40 of 165) with videos related to
Sort By:
Page
of 17
Behavioral Medicine (Washington, D.C.)
|
October 29, 2005
Surveillance behavior and prophylactic surgery after predictive testing for hereditary breast/ovarian cancer
Erna Claes, Gerry Evers-Kiebooms, Marleen Decruyenaere, et al.
Pediatric Dermatology
|
February 11, 2026
Novel Identical Likely Pathogenic ACTB Variant in Congenital Smooth Muscle Hamartoma: A Report of Two Pediatric Cases
Caroline Colmant, Eric Legius, Ifigenia Spanoudi-Kitrimi, et al.
Revue Medicale Suisse
|
March 26, 2026
[Pigmentary mosaicism: a literature review]
Selin Yener, Jean-Marc Good, Daniel Hohl, et al.
Neurology
|
November 1, 2015
Behavioral and cognitive outcomes for clinical trials in children with neurofibromatosis type 1
Thijs van der Vaart, André B Rietman, Ellen Plasschaert, et al.
European Journal of Endocrinology
|
September 15, 2023
Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families
Axelle Vuylsteke, Laurens Hannes, Hilde Brems, et al.
Nature Communications
|
February 22, 2023
SREBP modulates the NADP<sup>+</sup>/NADPH cycle to control night sleep in Drosophila
Vittoria Mariano, Alexandros K Kanellopoulos, Giuseppe Aiello, et al.
Pediatric Blood & Cancer
|
August 4, 2005
Therapy-related acute myeloid leukemia in a child with Noonan syndrome and clonal duplication of the germline PTPN11 mutation
Christophe F Chantrain, Priscilla Jijon, Thomas De Raedt, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society
|
December 4, 2009
Does paclitaxel-carboplatin chemotherapy in a dose-dense regimen enhance survival of BRCA-related ovarian cancer patients?
Karin Leunen, Isabelle Cadron, Toon Van Gorp, et al.
Surgical Neurology International
|
December 17, 2013
What the neurosurgeon should know about hemangioblastoma, both sporadic and in Von Hippel-Lindau disease: A literature review
Sven Bamps, Frank Van Calenbergh, Steven De Vleeschouwer, et al.
European Journal of Human Genetics : EJHG
|
August 13, 2002
Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD)
Geneviève Michils, Sabine Tejpar, Jean-Pierre Fryns, et al.
Page
of 17