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The Journal of Investigative Dermatology
|
May 1, 2015
MMP-10 Regulates Collagenolytic Activity of Alternatively Activated Resident Macrophages
Maryam G Rohani, Ryan S McMahan, Maria V Razumova, et al.
International Journal of Legal Medicine
|
December 4, 2014
Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases
C L Hertz, S L Christiansen, L Ferrero-Miliani, et al.
Journal of Medical Genetics
|
December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
S Lebon, M Chol, P Benit, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 12, 2001
Functional imaging in the work-up of childhood epilepsy
L Hertz-Pannier, C Chiron, P Véra, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
July 9, 2024
Strategies for DPYD testing prior to fluoropyrimidine chemotherapy in the US
Tabea Tracksdorf, D Max Smith, Skyler Pearse, et al.
Neuroradiology
|
April 19, 2003
Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation
N Boddaert, O Klein, N Ferguson, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|
April 23, 2024
Recommendations for pharmacogenetic testing in clinical practice guidelines in the US
Daniel L Hertz, Chad A Bousman, Howard L McLeod, et al.
Breast Cancer Research and Treatment
|
May 13, 2025
Tolerance for chemotherapy-induced peripheral neuropathy among women with metastatic breast cancer: a discrete-choice experiment
Rotana M Radwan, Anne L R Schuster, Daniel L Hertz, et al.
American Journal of Epidemiology
|
December 19, 2016
Cytochrome P-450 2D6 (CYP2D6) Genotype and Breast Cancer Recurrence in Tamoxifen-Treated Patients: Evaluating the Importance of Loss of Heterozygosity
Thomas P Ahern, Daniel L Hertz, Per Damkier, et al.
Journal of Medical Genetics
|
March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol, S Lebon, P Bénit, et al.
Page
of 37
Search research articles
Search
Showing results (301-310 of 368) with videos related to
Sort By:
Page
of 37
The Journal of Investigative Dermatology
|
May 1, 2015
MMP-10 Regulates Collagenolytic Activity of Alternatively Activated Resident Macrophages
Maryam G Rohani, Ryan S McMahan, Maria V Razumova, et al.
International Journal of Legal Medicine
|
December 4, 2014
Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases
C L Hertz, S L Christiansen, L Ferrero-Miliani, et al.
Journal of Medical Genetics
|
December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency
S Lebon, M Chol, P Benit, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 12, 2001
Functional imaging in the work-up of childhood epilepsy
L Hertz-Pannier, C Chiron, P Véra, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
July 9, 2024
Strategies for DPYD testing prior to fluoropyrimidine chemotherapy in the US
Tabea Tracksdorf, D Max Smith, Skyler Pearse, et al.
Neuroradiology
|
April 19, 2003
Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation
N Boddaert, O Klein, N Ferguson, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|
April 23, 2024
Recommendations for pharmacogenetic testing in clinical practice guidelines in the US
Daniel L Hertz, Chad A Bousman, Howard L McLeod, et al.
Breast Cancer Research and Treatment
|
May 13, 2025
Tolerance for chemotherapy-induced peripheral neuropathy among women with metastatic breast cancer: a discrete-choice experiment
Rotana M Radwan, Anne L R Schuster, Daniel L Hertz, et al.
American Journal of Epidemiology
|
December 19, 2016
Cytochrome P-450 2D6 (CYP2D6) Genotype and Breast Cancer Recurrence in Tamoxifen-Treated Patients: Evaluating the Importance of Loss of Heterozygosity
Thomas P Ahern, Daniel L Hertz, Per Damkier, et al.
Journal of Medical Genetics
|
March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol, S Lebon, P Bénit, et al.
Page
of 37