Search research articles
Contact Us
Filters
Showing results (121-130 of 167) with videos related to
Page
of 17
Sort By:
Nature Medicine
|
April 8, 2015
Corrigendum: Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1
Jean de la Croix Ndong, Alexander J Makowski, Sasidhar Uppuganti, et al.
The Journal of Pediatrics
|
January 14, 2012
Gastrointestinal bleeding in infantile hemangioma: a complication of segmental, rather than multifocal, infantile hemangiomas
Beth A Drolet, Elena Pope, Anna M Juern, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: new frontiers
Joseph L Kissil, Jaishri O Blakeley, Rosalie E Ferner, et al.
Journal of Pediatric Orthopedics
|
August 28, 2020
Are Some Randomized Clinical Trials Impossible?
Jonathan J Rios, B Stephens Richards, David A Stevenson, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2018
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation
Whitney L Wooderchak-Donahue, Peter Johnson, Jamie McDonald, et al.
Pediatric Transplantation
|
July 2, 2019
Cardiac transplantation in children with Noonan syndrome
Leslie M McCallen, Rebecca K Ameduri, Susan W Denfield, et al.
Neurology
|
July 7, 2021
Reliability of Handheld Dynamometry to Measure Focal Muscle Weakness in Neurofibromatosis Types 1 and 2
Srivandana Akshintala, Nashwa Khalil, Kaleb Yohay, et al.
Clinical Trials (London, England)
|
September 29, 2023
Potential endpoints for assessment of bone health in persons with neurofibromatosis type 1
Andrea M Gross, Scott R Plotkin, Nelson B Watts, et al.
HGG Advances
|
February 4, 2021
Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome
Emma Wakeling, Meriel McEntagart, Michael Bruccoleri, et al.
American Journal of Medical Genetics. Part A
|
December 23, 2011
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
Eric A Muller, Swaroop Aradhya, Joan F Atkin, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 167) with videos related to
Sort By:
Page
of 17
Nature Medicine
|
April 8, 2015
Corrigendum: Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1
Jean de la Croix Ndong, Alexander J Makowski, Sasidhar Uppuganti, et al.
The Journal of Pediatrics
|
January 14, 2012
Gastrointestinal bleeding in infantile hemangioma: a complication of segmental, rather than multifocal, infantile hemangiomas
Beth A Drolet, Elena Pope, Anna M Juern, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2010
What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: new frontiers
Joseph L Kissil, Jaishri O Blakeley, Rosalie E Ferner, et al.
Journal of Pediatric Orthopedics
|
August 28, 2020
Are Some Randomized Clinical Trials Impossible?
Jonathan J Rios, B Stephens Richards, David A Stevenson, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2018
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation
Whitney L Wooderchak-Donahue, Peter Johnson, Jamie McDonald, et al.
Pediatric Transplantation
|
July 2, 2019
Cardiac transplantation in children with Noonan syndrome
Leslie M McCallen, Rebecca K Ameduri, Susan W Denfield, et al.
Neurology
|
July 7, 2021
Reliability of Handheld Dynamometry to Measure Focal Muscle Weakness in Neurofibromatosis Types 1 and 2
Srivandana Akshintala, Nashwa Khalil, Kaleb Yohay, et al.
Clinical Trials (London, England)
|
September 29, 2023
Potential endpoints for assessment of bone health in persons with neurofibromatosis type 1
Andrea M Gross, Scott R Plotkin, Nelson B Watts, et al.
HGG Advances
|
February 4, 2021
Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome
Emma Wakeling, Meriel McEntagart, Michael Bruccoleri, et al.
American Journal of Medical Genetics. Part A
|
December 23, 2011
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
Eric A Muller, Swaroop Aradhya, Joan F Atkin, et al.
Page
of 17