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American Journal of Medical Genetics. Part A
|
June 20, 2017
Characterization of thrombosis in patients with Proteus syndrome
Kim M Keppler-Noreuil, Jay N Lozier, Julie C Sapp, et al.
Der Unfallchirurg
|
March 7, 2020
[Gluteal compartment syndrome after immobilization following opioid abuse]
J Gleich, J Fürmetz, C Kamla, et al.
Birth Defects Research
|
September 20, 2018
Descriptive epidemiology of cerebellar hypoplasia in the National Birth Defects Prevention Study
Meredith M Howley, Kim M Keppler-Noreuil, Christopher M Cunniff, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2011
Clinical insights gained from eight new cases and review of reported cases with Jeune syndrome (asphyxiating thoracic dystrophy)
Kim M Keppler-Noreuil, Margaret P Adam, Judy Welch, et al.
Dermatologic Clinics
|
November 29, 2016
Mosaic Disorders of the PI3K/PTEN/AKT/TSC/mTORC1 Signaling Pathway
Neera Nathan, Kim M Keppler-Noreuil, Leslie G Biesecker, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 7, 2019
A dyadic genotype-phenotype approach to diagnostic criteria for Proteus syndrome
Julie C Sapp, Anna Buser, Jasmine Burton-Akright, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 19, 2016
Somatic overgrowth disorders of the PI3K/AKT/mTOR pathway & therapeutic strategies
Kim M Keppler-Noreuil, Victoria E R Parker, Thomas N Darling, et al.
Archives of Orthopaedic and Trauma Surgery
|
December 23, 2024
Fulfillment of expectations and patient satisfaction following surgical treatment of complex proximal tibial fractures
L Keppler, F Navarre, A M Keppler, et al.
Injury
|
February 9, 2020
Postoperative physical activity in orthogeriatric patients - new insights with continuous monitoring
Alexander M Keppler, Jenny Holzschuh, Daniel Pfeufer, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2016
Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis
Kim M Keppler-Noreuil, Eva H Baker, Julie C Sapp, et al.
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of 10
Search research articles
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Showing results (11-20 of 92) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics. Part A
|
June 20, 2017
Characterization of thrombosis in patients with Proteus syndrome
Kim M Keppler-Noreuil, Jay N Lozier, Julie C Sapp, et al.
Der Unfallchirurg
|
March 7, 2020
[Gluteal compartment syndrome after immobilization following opioid abuse]
J Gleich, J Fürmetz, C Kamla, et al.
Birth Defects Research
|
September 20, 2018
Descriptive epidemiology of cerebellar hypoplasia in the National Birth Defects Prevention Study
Meredith M Howley, Kim M Keppler-Noreuil, Christopher M Cunniff, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2011
Clinical insights gained from eight new cases and review of reported cases with Jeune syndrome (asphyxiating thoracic dystrophy)
Kim M Keppler-Noreuil, Margaret P Adam, Judy Welch, et al.
Dermatologic Clinics
|
November 29, 2016
Mosaic Disorders of the PI3K/PTEN/AKT/TSC/mTORC1 Signaling Pathway
Neera Nathan, Kim M Keppler-Noreuil, Leslie G Biesecker, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 7, 2019
A dyadic genotype-phenotype approach to diagnostic criteria for Proteus syndrome
Julie C Sapp, Anna Buser, Jasmine Burton-Akright, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
November 19, 2016
Somatic overgrowth disorders of the PI3K/AKT/mTOR pathway & therapeutic strategies
Kim M Keppler-Noreuil, Victoria E R Parker, Thomas N Darling, et al.
Archives of Orthopaedic and Trauma Surgery
|
December 23, 2024
Fulfillment of expectations and patient satisfaction following surgical treatment of complex proximal tibial fractures
L Keppler, F Navarre, A M Keppler, et al.
Injury
|
February 9, 2020
Postoperative physical activity in orthogeriatric patients - new insights with continuous monitoring
Alexander M Keppler, Jenny Holzschuh, Daniel Pfeufer, et al.
American Journal of Medical Genetics. Part A
|
August 24, 2016
Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis
Kim M Keppler-Noreuil, Eva H Baker, Julie C Sapp, et al.
Page
of 10