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Journal of the International Neuropsychological Society : JINS
|
November 17, 2012
Neuropsychological profiles of children with aqueductal stenosis and Spina Bifida myelomeningocele
Lyla E Hampton, Jack M Fletcher, Paul Cirino, et al.
Journal of Medical Genetics
|
January 23, 2025
Homozygous missense variant in <i>C2orf69</i> causes early-onset neurodegeneration, leukoencephalopathy and autoinflammation
Rachel Youjin Oh, Michael Maier, Susan Blaser, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features
Arie Koifman, Annette Feigenbaum, Weimin Bi, et al.
The Journal of Otolaryngology
|
August 8, 2008
Dilated endolymphatic fossae in a 2800-year-old Egyptian mummy
Evan J Propst, Susan Blaser, Stephanie Holowka, et al.
Medical and Pediatric Oncology
|
March 29, 2002
Predilection of retinoblastoma metastases for the mandible
Jayshree Pandya, Kathia Valverde, Elise Heon, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 20, 2009
Malformations of the fetal dural sinuses
Matthew McInnes, Katherine Fong, Andrea Grin, et al.
Thrombosis Research
|
September 15, 2007
Epidural hematoma following tissue plasminogen activator (tPA) therapy for pulmonary embolism in a pediatric patient with stage IV Burkitt's lymphoma: a case report
Patcharee Komvilaisak, Ronald Grant, Sheila Weitzman, et al.
The Laryngoscope
|
June 10, 2009
Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes
John R de Almeida, Adrian L James, Blake C Papsin, et al.
The Journal of Physical Chemistry Letters
|
April 7, 2020
Locating Cytosine Conical Intersections by Laser Experiments and <i>Ab Initio</i> Calculations
Maria A Trachsel, Susan Blaser, Simon Lobsiger, et al.
Molecular Genetics and Metabolism Reports
|
October 26, 2020
Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a <i>PEX3</i> defect: Case report and literature review
Whiwon Lee, Gregory Costain, Susan Blaser, et al.
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of 18
Search research articles
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Showing results (81-90 of 177) with videos related to
Sort By:
Page
of 18
Journal of the International Neuropsychological Society : JINS
|
November 17, 2012
Neuropsychological profiles of children with aqueductal stenosis and Spina Bifida myelomeningocele
Lyla E Hampton, Jack M Fletcher, Paul Cirino, et al.
Journal of Medical Genetics
|
January 23, 2025
Homozygous missense variant in <i>C2orf69</i> causes early-onset neurodegeneration, leukoencephalopathy and autoinflammation
Rachel Youjin Oh, Michael Maier, Susan Blaser, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2010
A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features
Arie Koifman, Annette Feigenbaum, Weimin Bi, et al.
The Journal of Otolaryngology
|
August 8, 2008
Dilated endolymphatic fossae in a 2800-year-old Egyptian mummy
Evan J Propst, Susan Blaser, Stephanie Holowka, et al.
Medical and Pediatric Oncology
|
March 29, 2002
Predilection of retinoblastoma metastases for the mandible
Jayshree Pandya, Kathia Valverde, Elise Heon, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 20, 2009
Malformations of the fetal dural sinuses
Matthew McInnes, Katherine Fong, Andrea Grin, et al.
Thrombosis Research
|
September 15, 2007
Epidural hematoma following tissue plasminogen activator (tPA) therapy for pulmonary embolism in a pediatric patient with stage IV Burkitt's lymphoma: a case report
Patcharee Komvilaisak, Ronald Grant, Sheila Weitzman, et al.
The Laryngoscope
|
June 10, 2009
Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes
John R de Almeida, Adrian L James, Blake C Papsin, et al.
The Journal of Physical Chemistry Letters
|
April 7, 2020
Locating Cytosine Conical Intersections by Laser Experiments and <i>Ab Initio</i> Calculations
Maria A Trachsel, Susan Blaser, Simon Lobsiger, et al.
Molecular Genetics and Metabolism Reports
|
October 26, 2020
Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a <i>PEX3</i> defect: Case report and literature review
Whiwon Lee, Gregory Costain, Susan Blaser, et al.
Page
of 18