Search research articles
Contact Us
Filters
Showing results (451-460 of 889) with videos related to
Page
of 89
Sort By:
The American Journal of Tropical Medicine and Hygiene
|
March 30, 2016
Human Infections by Multiple Spotted Fever Group Rickettsiae in Tennessee
Josie Delisle, Nicole L Mendell, Annica Stull-Lane, et al.
Brain Structure & Function
|
June 11, 2016
Expansion of mossy fibers and CA3 apical dendritic length accompanies the fall in dendritic spine density after gonadectomy in male, but not female, rats
Ari L Mendell, Sarah Atwi, Craig D C Bailey, et al.
Environmental Research
|
November 20, 2021
Residential bacteria and fungi identified by high-throughput sequencing and childhood respiratory health
Jennie Cox, Timothy Stone, Patrick Ryan, et al.
Neurology
|
December 31, 1997
Quality improvement in neurology residency programs. Report of the Quality Improvement Committee of the Association of University Professors of Neurology
W G Bradley, J Daube, J R Mendell, et al.
American Journal of Human Genetics
|
May 1, 1992
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers
C J Klein, D D Coovert, D E Bulman, et al.
Dermatology and Therapy
|
September 21, 2022
Unmet Need in People with Psoriasis and Skin of Color in Canada and the United States
Geeta Yadav, Jensen Yeung, Yvette Miller-Monthrope, et al.
Clinical Pharmacology in Drug Development
|
June 6, 2018
Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Mirogabalin When Coadministered With Lorazepam, Zolpidem, Tramadol, or Ethanol: Results From Drug-Drug Interaction Studies in Healthy Subjects
Mendel Jansen, Jeanne Mendell, Alexander Currie, et al.
American Journal of Human Genetics
|
December 5, 1998
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number
D W Parsons, P E McAndrew, S T Iannaccone, et al.
Human Molecular Genetics
|
November 1, 1996
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene
D W Parsons, P E McAndrew, U R Monani, et al.
Muscle & Nerve
|
July 18, 2009
Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm "Hirayama disease"
Bakri Elsheikh, John T Kissel, Gregory Christoforidis, et al.
Page
of 89
Search research articles
Search
Showing results (451-460 of 889) with videos related to
Sort By:
Page
of 89
The American Journal of Tropical Medicine and Hygiene
|
March 30, 2016
Human Infections by Multiple Spotted Fever Group Rickettsiae in Tennessee
Josie Delisle, Nicole L Mendell, Annica Stull-Lane, et al.
Brain Structure & Function
|
June 11, 2016
Expansion of mossy fibers and CA3 apical dendritic length accompanies the fall in dendritic spine density after gonadectomy in male, but not female, rats
Ari L Mendell, Sarah Atwi, Craig D C Bailey, et al.
Environmental Research
|
November 20, 2021
Residential bacteria and fungi identified by high-throughput sequencing and childhood respiratory health
Jennie Cox, Timothy Stone, Patrick Ryan, et al.
Neurology
|
December 31, 1997
Quality improvement in neurology residency programs. Report of the Quality Improvement Committee of the Association of University Professors of Neurology
W G Bradley, J Daube, J R Mendell, et al.
American Journal of Human Genetics
|
May 1, 1992
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers
C J Klein, D D Coovert, D E Bulman, et al.
Dermatology and Therapy
|
September 21, 2022
Unmet Need in People with Psoriasis and Skin of Color in Canada and the United States
Geeta Yadav, Jensen Yeung, Yvette Miller-Monthrope, et al.
Clinical Pharmacology in Drug Development
|
June 6, 2018
Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Mirogabalin When Coadministered With Lorazepam, Zolpidem, Tramadol, or Ethanol: Results From Drug-Drug Interaction Studies in Healthy Subjects
Mendel Jansen, Jeanne Mendell, Alexander Currie, et al.
American Journal of Human Genetics
|
December 5, 1998
Intragenic telSMN mutations: frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy number
D W Parsons, P E McAndrew, S T Iannaccone, et al.
Human Molecular Genetics
|
November 1, 1996
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene
D W Parsons, P E McAndrew, U R Monani, et al.
Muscle & Nerve
|
July 18, 2009
Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm "Hirayama disease"
Bakri Elsheikh, John T Kissel, Gregory Christoforidis, et al.
Page
of 89