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Case reports in orthopedics, ISSN 2090-6749, 2018, Volume 2018, pp. 8136150 - 6
Osteomyelitis caused by species may be difficult to diagnose and treat. We report a case of treatment for osteomyelitis caused by species in the epiphysis of... 
Osteomyelitis | Care and treatment | Medical examination | Vaccination | BCG | BCG vaccines | Antitubercular agents | Diagnosis | Endoscopy | Blood | Knee | Pathogens | Immunization | Nuclear magnetic resonance--NMR | Joint surgery | Chemotherapy | Infectious diseases | Tuberculosis | Preschool children | Consent | Surgery | Gangrene
Journal Article
Journal of Nihon University Medical Association, ISSN 0029-0424, 06/2018, Volume 77, Issue 3, pp. 165 - 168
Journal Article
Journal of Nucleic Acids, ISSN 2090-0201, 2011, Volume 2011, pp. 103872 - 6
Remote control of aptamer function has allowed us to control protein function in space and time. Here, we propose a novel control system for aptamer function... 
Physiological aspects | Protein engineering | Thrombin | Research | Magnetic fields
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2011, Volume 155, Issue 8, pp. 1949 - 1958
Loss‐of‐function mutations in CHST14, dermatan 4‐O‐sulfotransferase 1 (D4ST1) deficiency, have recently been found to cause adducted thumb‐clubfoot syndrome... 
dermatan 4‐O‐sulfotransferase 1 deficiency | malformations | congenital contractures | progressive multisystem fragility‐related manifestations | musculocontractural Ehlers–Danlos syndrome | adducted thumb‐clubfoot syndrome | Ehlers–Danlos syndrome Kosho type | Malformations | Musculocontractural Ehlers-Danlos syndrome | Congenital contractures | Adducted thumb-clubfoot syndrome | Ehlers-Danlos syndrome Kosho type | Dermatan 4-O-sulfotransferase 1 deficiency | Progressive multisystem fragility-related manifestations | dermatan 4-O-sulfotransferase 1 deficiency | ADDUCTED THUMB | CONTRACTURES | musculocontractural Ehlers-Danlos syndrome | DERMATAN-4-SULFOTRANSFERASE | adducted thumb-clubfoot syndrome | VIB | GENE | GENETICS & HEREDITY | CLUB FOOT SYNDROME | progressive multisystem fragility-related manifestations | MUTATIONS | CHST14 | JOINT | Sulfotransferases - genetics | Genetic Association Studies | Humans | Child, Preschool | Male | Developmental Disabilities - genetics | Sulfotransferases - deficiency | Ehlers-Danlos Syndrome - genetics | Phenotype | DNA Mutational Analysis | Clubfoot - surgery | Child | Cryptorchidism - genetics | Ehlers-Danlos Syndrome - enzymology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Heart | Ehlers-Danlos syndrome | Congenital defects | Central nervous system | Birth | Procollagen-lysine 5-dioxygenase | Kidney | Dislocation | Fibrillogenesis | Collagen | Hematoma | Skin | Children | Mutation | Joints | Age
Journal Article
Japanese Journal of Gastroenterological Surgery, ISSN 0386-9768, 2015, Volume 48, Issue 4, pp. 328 - 336
Journal Article
Journal Article
Japanese Journal of Gastroenterological Surgery, ISSN 0386-9768, 2013, Volume 46, Issue 8, pp. 626 - 633
Journal Article
Suizo, ISSN 0913-0071, 2013, Volume 28, Issue 2, pp. 191 - 196
Journal Article
Suizo, ISSN 0913-0071, 2013, Volume 28, Issue 6, pp. 699 - 706
Journal Article
Japanese Journal of Gastroenterological Surgery, ISSN 0386-9768, 2010, Volume 43, Issue 6, pp. 654 - 660
Journal Article
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