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Stroke
|
September 28, 2019
Siponimod (BAF-312) Attenuates Perihemorrhagic Edema And Improves Survival in Experimental Intracerebral Hemorrhage
Tobias Bobinger, Anatol Manaenko, Petra Burkardt, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2021
Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes
Filomena Pirozzi, Benson Lee, Nicole Horsley, et al.
HGG Advances
|
September 16, 2021
<i>PTPN4</i> germline variants result in aberrant neurodevelopment and growth
Joanna J Chmielewska, Deepika Burkardt, Jorge Luis Granadillo, et al.
Communications Biology
|
April 20, 2022
Evidence for postnatal neurogenesis in the human amygdala
Sebastian S Roeder, Petra Burkardt, Fabian Rost, et al.
Chemsuschem
|
October 8, 2021
Designed to Be Green, Economic, and Efficient: A Ketone-Ester-Alcohol-Alkane Blend for Future Spark-Ignition Engines
Philipp Ackermann, Karsten E Braun, Patrick Burkardt, et al.
Journal of Medical Genetics
|
November 17, 2020
Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?
Alessandra Pennisi, Agnès Rötig, Charles-Joris Roux, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2011
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25
Deepika D'Cunha Burkardt, Jill A Rosenfeld, Maria L Helgeson, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 28, 2025
Evidence-based classification of genes implicated in skeletal disorders using the ClinGen curation framework
Ryan F Webb, Hannah McCurry, Amanda Girod, et al.
American Journal of Medical Genetics. Part A
|
August 11, 2019
HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals
Deepika D'Cunha Burkardt, Anna Zachariou, Chey Loveday, et al.
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of 10
Search research articles
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Showing results (91-100 of 99) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 99 results.
Stroke
|
September 28, 2019
Siponimod (BAF-312) Attenuates Perihemorrhagic Edema And Improves Survival in Experimental Intracerebral Hemorrhage
Tobias Bobinger, Anatol Manaenko, Petra Burkardt, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2021
Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes
Filomena Pirozzi, Benson Lee, Nicole Horsley, et al.
HGG Advances
|
September 16, 2021
<i>PTPN4</i> germline variants result in aberrant neurodevelopment and growth
Joanna J Chmielewska, Deepika Burkardt, Jorge Luis Granadillo, et al.
Communications Biology
|
April 20, 2022
Evidence for postnatal neurogenesis in the human amygdala
Sebastian S Roeder, Petra Burkardt, Fabian Rost, et al.
Chemsuschem
|
October 8, 2021
Designed to Be Green, Economic, and Efficient: A Ketone-Ester-Alcohol-Alkane Blend for Future Spark-Ignition Engines
Philipp Ackermann, Karsten E Braun, Patrick Burkardt, et al.
Journal of Medical Genetics
|
November 17, 2020
Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?
Alessandra Pennisi, Agnès Rötig, Charles-Joris Roux, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2011
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25
Deepika D'Cunha Burkardt, Jill A Rosenfeld, Maria L Helgeson, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 28, 2025
Evidence-based classification of genes implicated in skeletal disorders using the ClinGen curation framework
Ryan F Webb, Hannah McCurry, Amanda Girod, et al.
American Journal of Medical Genetics. Part A
|
August 11, 2019
HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals
Deepika D'Cunha Burkardt, Anna Zachariou, Chey Loveday, et al.
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of 10