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Plastic and Reconstructive Surgery
|
January 1, 2009
Comparison of computed tomographic imaging measurements with clinical findings in children with unilateral lambdoid synostosis
Emilia A Ploplys, Richard A Hopper, Arshad R Muzaffar, et al.
Fetal and Pediatric Pathology
|
April 20, 2019
Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review
Christian Peña-Padilla, Lorena Viramontes-Aguilar, Gerónimo Tavares-Macías, et al.
Journal of Neurosurgery
|
May 10, 2008
Presurgical and postsurgical assessment of the neurodevelopment of infants with single-suture craniosynostosis: comparison with controls
Jacqueline R Starr, Kathleen A Kapp-Simon, Yona Keich Cloonan, et al.
AJNR. American Journal of Neuroradiology
|
March 27, 2025
Revisiting a Rare Anomaly Described 25 Years Ago in the AJNR: A Journey from Pediatric Hemifacial Microsomia and Middle Cranial Fossa Aplasia to CSF-Lymphatic Fistula and Spontaneous Intracranial Hypotension as an Adult
Andrew L Callen, Ashoke R Khanwalkar, Michael L Cunningham, et al.
Toxicology and Applied Pharmacology
|
October 24, 2007
Time course investigation of PPARalpha- and Kupffer cell-dependent effects of WY-14,643 in mouse liver using microarray gene expression
Courtney G Woods, Oksana Kosyk, Blair U Bradford, et al.
Neurosurgery
|
July 21, 2010
Little evidence of association between severity of trigonocephaly and cognitive development in infants with single-suture metopic synostosis
Jacqueline R Starr, H Jill Lin, Salvador Ruiz-Correa, et al.
Neurosurgery
|
September 18, 2008
New severity indices for quantifying single-suture metopic craniosynostosis
Salvador Ruiz-Correa, Jacqueline R Starr, H Jill Lin, et al.
The Laryngoscope
|
September 5, 2020
Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice
Austin S Lam, Carrie C Liu, Gail H Deutsch, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2013
Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
Yasuhiro Kido, Christopher T Gordon, Satoru Sakazume, et al.
Critical Reviews in Toxicology
|
November 5, 2013
Mode of action framework analysis for receptor-mediated toxicity: The peroxisome proliferator-activated receptor alpha (PPARα) as a case study
J Christopher Corton, Michael L Cunningham, B Timothy Hummer, et al.
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of 17
Search research articles
Search
Showing results (101-110 of 162) with videos related to
Sort By:
Page
of 17
Plastic and Reconstructive Surgery
|
January 1, 2009
Comparison of computed tomographic imaging measurements with clinical findings in children with unilateral lambdoid synostosis
Emilia A Ploplys, Richard A Hopper, Arshad R Muzaffar, et al.
Fetal and Pediatric Pathology
|
April 20, 2019
Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review
Christian Peña-Padilla, Lorena Viramontes-Aguilar, Gerónimo Tavares-Macías, et al.
Journal of Neurosurgery
|
May 10, 2008
Presurgical and postsurgical assessment of the neurodevelopment of infants with single-suture craniosynostosis: comparison with controls
Jacqueline R Starr, Kathleen A Kapp-Simon, Yona Keich Cloonan, et al.
AJNR. American Journal of Neuroradiology
|
March 27, 2025
Revisiting a Rare Anomaly Described 25 Years Ago in the AJNR: A Journey from Pediatric Hemifacial Microsomia and Middle Cranial Fossa Aplasia to CSF-Lymphatic Fistula and Spontaneous Intracranial Hypotension as an Adult
Andrew L Callen, Ashoke R Khanwalkar, Michael L Cunningham, et al.
Toxicology and Applied Pharmacology
|
October 24, 2007
Time course investigation of PPARalpha- and Kupffer cell-dependent effects of WY-14,643 in mouse liver using microarray gene expression
Courtney G Woods, Oksana Kosyk, Blair U Bradford, et al.
Neurosurgery
|
July 21, 2010
Little evidence of association between severity of trigonocephaly and cognitive development in infants with single-suture metopic synostosis
Jacqueline R Starr, H Jill Lin, Salvador Ruiz-Correa, et al.
Neurosurgery
|
September 18, 2008
New severity indices for quantifying single-suture metopic craniosynostosis
Salvador Ruiz-Correa, Jacqueline R Starr, H Jill Lin, et al.
The Laryngoscope
|
September 5, 2020
Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice
Austin S Lam, Carrie C Liu, Gail H Deutsch, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2013
Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
Yasuhiro Kido, Christopher T Gordon, Satoru Sakazume, et al.
Critical Reviews in Toxicology
|
November 5, 2013
Mode of action framework analysis for receptor-mediated toxicity: The peroxisome proliferator-activated receptor alpha (PPARα) as a case study
J Christopher Corton, Michael L Cunningham, B Timothy Hummer, et al.
Page
of 17