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Endocrine Journal, ISSN 0918-8959, 2017, Volume 64, Issue 3, pp. 283 - 289
Journal Article
Clinical Case Reports, ISSN 2050-0904, 12/2018, Volume 6, Issue 12, pp. 2371 - 2375
Hypopituitarism could have been overlooked so far in the patients with 9q subtelomere deletion syndrome (9q STDS ); thus, further investigations or... 
hypopituitarism | 9q subtelomere deletion syndrome | whole‐exome sequence | array comparative genomic hybridization | central adrenal insufficiency | whole-exome sequence | Pituitary gland | Genetic disorders
Journal Article
Endocrine Journal, ISSN 0918-8959, 2016
X-linked hypophosphatemia (XLH) is a group of rare disorders caused by defective proximal tubular reabsorption of phosphate. Mutations in the PHEX gene are... 
Hypertension | X-linked hypophosphatemia | Hypophosphatemic rickets | PHEX | Hyperparathyroidism
Journal Article
Clinical Pediatric Endocrinology, ISSN 0918-5739, 2016, Volume 25, Issue 4, pp. 139 - 141
Journal Article
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 12/2018, Volume 7, Issue 12, p. 479
Osteogenesis imperfecta (OI) is a connective tissue disorder that is characterized by low bone density leading to recurrent fractures. The efficacy of the... 
DENSITY | bone mineral density | MEDICINE, GENERAL & INTERNAL | PAMIDRONATE | TURNOVER | PHASE-2 | osteogenesis imperfecta | osteoporosis | POSTMENOPAUSAL WOMEN | denosumab | fractures | CHILDREN
Journal Article
Clinical Pediatric Endocrinology, ISSN 0918-5739, 2015, Volume 24, Issue 3, pp. 139 - 141
Journal Article
Clinical calcium, ISSN 0917-5857, 2013, Volume 23, Issue 10, pp. 1405 - 1412
Journal Article
Clinical Pediatric Endocrinology, ISSN 0918-5739, 2016, Volume 25, Issue 4, pp. 139 - 141
[Introduction] Neonatal diabetes mellitus (NDM), characterized by hyperglycemia and the need for insulin treatment within the first 6 mo of life, is a rare... 
Journal Article
Clinical Pediatric Endocrinology, ISSN 0918-5739, 2015, Volume 24, Issue 3, pp. 139 - 141
[Introduction] Spondyloepiphyseal dysplasia tarda (SEDT ; MIM # 313400) is a rare X-linked recessive skeletal disease characterized by disproportionate short... 
Journal Article
Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases, ISSN 0387-5911, 05/2008, Volume 82, Issue 3, pp. 177 - 181
Journal Article
Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases, ISSN 0387-5911, 2008, Volume 82, Issue 3, pp. 177 - 181
Journal Article
Nihon Shoni Jinzobyo Gakkai Zasshi, ISSN 0915-2245, 2018, Volume 31, Issue 2, pp. 167 - 171
Journal Article
Nihon Shoni Jinzobyo Gakkai Zasshi, ISSN 0915-2245, 2015, Volume 28, Issue 2, pp. 169 - 175
Journal Article
Clinical calcium, ISSN 0917-5857, 10/2013, Volume 23, Issue 10, p. 1405
Rickets is a condition of inadequate mineralization of osteoid and cartilage at the growing ends of bones in children. In this brief review, we first explained... 
Age Factors | Vitamin D Deficiency - complications | Humans | Vitamin D Deficiency - drug therapy | Rickets - physiopathology | Rickets - diagnosis | Calcium - blood | Vitamin D Deficiency - diagnosis | Rickets - metabolism | Bone and Bones - metabolism | Phosphates - blood | Rickets - etiology | Vitamin D Deficiency - etiology
Journal Article
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