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A red-shifted two-photon-only caging group for three-dimensional photorelease
A rare pediatric case of a thymic cytotoxic and lymphoblastic T/NK cell lymphoma

Human papilloma virus and esophageal carcinoma in a Latin-American region
Screening red foxes (Vulpes vulpes) for possible viral causes of encephalitis

HÁBITOS ALIMENTARES EM PEIXES DE ÁGUA DOCE: UMA REVISÃO SOBRE METODOLOGIAS E ESTUDOS EM VÁRZEAS BRASILEIRAS
Poster Session A

4th Pediatric Allergy and Asthma Meeting (PAAM)
Analysis of Various Factors and Techniques to Improve Outcome of Surgical Management of 243 Cases of CSF Rhinorrhea

Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report
Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort

Cerebral damage in neonates resulting from arteriovenous malformation of the vein of Galen
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5q.

Effect of Cellular Therapy in Progression of Becker’s Muscular Dystrophy: A Case Study
Surgical treatment of aspergillus spondylodiscitis

Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene.
2013 European Thyroid Association Guidelines for the Diagnosis and Treatment of Thyrotropin-Secreting Pituitary Tumors

A Case of Oral Myiasis Caused by Lucilia sericata (Diptera: Calliphoridae) in Korea
“Pathologic” Fractures: Should These Be Included in Epidemiologic Studies of Osteoporotic Fractures?

Novel Mutations in the CLCN1 Gene of Myotonia Congenita: 2 Case Reports
Bone grafting with granular biomaterial in segmental maxillary osteotomy: A case report

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