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Italian Journal of Pediatrics|October 14, 2017
Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: a case reportStefania Moia, Daniele Tessaris, Silvia Einaudi, et al.
Molecular Medicine (Cambridge, Mass.)|December 29, 2000
Induction of skin fibrosis in mice expressing a mutated fibrillin-1 geneS Saito, H Nishimura, R G Phelps, et al.
Arthritis and Rheumatism|October 18, 2002
Halofuginone inhibition of COL1A2 promoter activity via a c-Jun-dependent mechanismTracy L McGaha, Takao Kodera, Harry Spiera, et al.
Annals of Clinical and Laboratory Science|May 1, 1993
Reemergence of the International Normalized Ratio for the standardization of prothrombin timeE E Morse, S Panek, P Pisciotto, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|October 23, 2016
Intimacy, Substance Use, and Communication Needs During Cancer Therapy: A Report From the "Resilience in Adolescents and Young Adults" StudyAbby R Rosenberg, Kira Bona, Tyler Ketterl, et al.
American Journal of Ophthalmology|May 23, 2015
Punctal Plug Retention Rates for the Treatment of Moderate to Severe Dry Eye: A Randomized, Double-Masked, Controlled Clinical TrialAshley R Brissette, Zale D Mednick, Kelly D Schweitzer, et al.
Journal of Autoimmunity|February 6, 1998
B-cell deficiency does not abrogate development of cutaneous hyperplasia in mice inheriting the defective fibrillin-1 geneK N Kasturi, A Hatakeyama, C Murai, et al.
Transplantation Proceedings|September 25, 2007
The concept of quality of life in organ transplantationP Burra, M De Bona, G Germani, et al.
International Forum of Allergy & Rhinology|May 26, 2017
The effect of allergen immunotherapy in the onset of new sensitizations: a meta-analysisGabriele Di Lorenzo, Maria Stefania Leto-Barone, Simona La Piana, et al.
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