Výsledky vyhledávání - "Spencer M. Vale"

Knowledge of dermatologic abbreviations: A survey of patients and physicians who are not dermatologists

Autor: Kari L. Martin, Susan K Ailor, Spencer M. Vale, Kelly Koenig

Publikováno v: Journal of the American Academy of Dermatology. 76:362-364

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a9fd854f52a22e1c47560465393abdd
https://doi.org/10.1016/j.jaad.2016.08.050

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Pharmacoeconomic Considerations in Treating Actinic Keratosis: An Update

Autor: Spencer M. Vale, Dane Hill, Steven R. Feldman

Publikováno v: PharmacoEconomics. 35(2)

Actinic keratosis is one of the most common dermatological diagnoses worldwide, especially among the elderly, fair-skinned, and immunocompromised, and is associated with a risk of transformation to skin cancer. With actinic keratosis and skin cancer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f2ada9e72d98d7556b83d30eacde8a
https://pubmed.ncbi.nlm.nih.gov/27785771

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Transgenic inactivation of murine myostatin does not decrease the severity of disease in a model of Spinal Muscular Atrophy

Autor: Megan M. Krogman, Christian L. Lorson, Michael L. Garcia, Ferrill F. Rose, Hansjörg Rindt, Spencer M. Vale, Desire M. Buckley

Publikováno v: Neuromuscular Disorders. 22:277-285

Spinal Muscular Atrophy (SMA) is a devastating neurodegenerative disease and is a leading genetic cause of infantile death. SMA is caused by the homozygous loss of Survival Motor Neuron-1 (SMN1). The presence of a nearly identical copy gene called SM

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cd437dedc670b62ac61fe4ca1039cf1
https://doi.org/10.1016/j.nmd.2011.10.012

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Cardiac defects contribute to the pathology of spinal muscular atrophy models

Autor: Will A. Sewell, Christian L. Lorson, Javad Habibi, Hsiao T. Yang, Spencer M. Vale, Monir Shababi

Publikováno v: Human molecular genetics. 19(20)

Spinal muscular atrophy (SMA) is an autosomal recessive disorder, which is the leading genetic cause of infantile death. SMA is the most common inherited motor neuron disease and occurs in approximately 1:6000 live births. The gene responsible for SM

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dce1dd00fbee439efdbfc8a06dec95f
https://pubmed.ncbi.nlm.nih.gov/20696672

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