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Pediatrics
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April 3, 2004
Wilms tumor screening is unnecessary in Klippel-Trenaunay syndrome
Arin K Greene, Mark Kieran, Patricia E Burrows, et al.
The Journal of Clinical Investigation
|
June 1, 1994
Cellular markers that distinguish the phases of hemangioma during infancy and childhood
K Takahashi, J B Mulliken, H P Kozakewich, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 28, 2009
Treatment of unilateral coronal synostosis by endoscopic strip craniectomy or fronto-orbital advancement: Ophthalmologic findings
Sarah MacKinnon, Gary F Rogers, Matt Gregas, et al.
Skeletal Radiology
|
February 2, 2013
Gorham-Stout disease and generalized lymphatic anomaly--clinical, radiologic, and histologic differentiation
Shailee Lala, John B Mulliken, Ahmad I Alomari, et al.
Journal of Cell Science
|
April 23, 1999
The role of matrix metalloproteinase activity in the maturation of human capillary endothelial cells in vitro
B M Kräling, D G Wiederschain, T Boehm, et al.
International Journal of Oncology
|
February 20, 1999
Progressive growth of infantile cutaneous hemangiomas is directly correlated with hyperplasia and angiogenesis of adjacent epidermis and inversely correlated with expression of the endogenous angiogenesis inhibitor, IFN-beta
D R Bielenberg, C D Bucana, R Sanchez, et al.
The Journal of Craniofacial Surgery
|
October 10, 2009
Cleft palate in Pfeiffer syndrome
Joan M Stoler, Heather Rosen, Urmen Desai, et al.
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences
|
June 12, 2012
Cerebrofacial venous anomalies, sinus pericranii, ocular abnormalities and developmental delay
B Macit, P E Burrows, S Yilmaz, et al.
Annals of Plastic Surgery
|
June 2, 2011
Venous malformation: risk of progression during childhood and adolescence
Aladdin H Hassanein, John B Mulliken, Steven J Fishman, et al.
Clinical Genetics
|
September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations
A Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Page
of 49
Search research articles
Search
Showing results (311-320 of 481) with videos related to
Sort By:
Page
of 49
Pediatrics
|
April 3, 2004
Wilms tumor screening is unnecessary in Klippel-Trenaunay syndrome
Arin K Greene, Mark Kieran, Patricia E Burrows, et al.
The Journal of Clinical Investigation
|
June 1, 1994
Cellular markers that distinguish the phases of hemangioma during infancy and childhood
K Takahashi, J B Mulliken, H P Kozakewich, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 28, 2009
Treatment of unilateral coronal synostosis by endoscopic strip craniectomy or fronto-orbital advancement: Ophthalmologic findings
Sarah MacKinnon, Gary F Rogers, Matt Gregas, et al.
Skeletal Radiology
|
February 2, 2013
Gorham-Stout disease and generalized lymphatic anomaly--clinical, radiologic, and histologic differentiation
Shailee Lala, John B Mulliken, Ahmad I Alomari, et al.
Journal of Cell Science
|
April 23, 1999
The role of matrix metalloproteinase activity in the maturation of human capillary endothelial cells in vitro
B M Kräling, D G Wiederschain, T Boehm, et al.
International Journal of Oncology
|
February 20, 1999
Progressive growth of infantile cutaneous hemangiomas is directly correlated with hyperplasia and angiogenesis of adjacent epidermis and inversely correlated with expression of the endogenous angiogenesis inhibitor, IFN-beta
D R Bielenberg, C D Bucana, R Sanchez, et al.
The Journal of Craniofacial Surgery
|
October 10, 2009
Cleft palate in Pfeiffer syndrome
Joan M Stoler, Heather Rosen, Urmen Desai, et al.
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences
|
June 12, 2012
Cerebrofacial venous anomalies, sinus pericranii, ocular abnormalities and developmental delay
B Macit, P E Burrows, S Yilmaz, et al.
Annals of Plastic Surgery
|
June 2, 2011
Venous malformation: risk of progression during childhood and adolescence
Aladdin H Hassanein, John B Mulliken, Steven J Fishman, et al.
Clinical Genetics
|
September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations
A Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Page
of 49