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in or near a center or constituting a center; the inner area; "a central position"
a workplace that serves as a telecommunications facility where lines from telephones can be connected together to permit communication (同)telephone exchange, exchange

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1. 思春期早発症の定義、原因、および評価 definition etiology and evaluation of precocious puberty
2. 思春期早発症の治療 treatment of precocious puberty
3. 小児癌生存者における内分泌障害 endocrinopathies in the childhood cancer survivor
4. 早期副腎皮質性第二次性徴 premature adrenarche
5. 小児における先天性中枢性低換気症候群および睡眠関連低換気症のその他の原因 congenital central hypoventilation syndrome and other causes of sleep related hypoventilation in children

Epidermolysis bullosa simplex with PLEC mutations: new phenotypes and new mutations.

Charlesworth A, Chiaverini C, Chevrant-Breton J, Delrio M, Diociaiuti A, Dupuis RP, El Hachem M, Le Fiblec B, Sankari-Ho AM, Valhquist A, Wierzbicka E, Lacour JP, Meneguzzi G.SourceFrench Centre for Hereditary Epidermolysis Bullosa, Archet 2 Hospital, Nice, France Department of Dermatology, CHU of Rennes, France CIEMAT-CIBER on Rare Diseases and Regenerative Medicine Unit-U714, Madrid, Spain Department of Dermatology, Hospital Bambin Gesù, Rome, Italy Department of Neonatology, and Department of Gynaecology, Le Foll Hospital, Saint Brieuc, France Department of Medical Sciences (Dermatology), Uppsala University, Uppsala, Sweden Department of Dermatology, Akademiska Hospital, Uppsala, Sweden Department of Dermatology, CHU of Poitiers, France Faculty of Medicine, University of Nice-Sophia Antipolis, Nice, France CNRS UMR 7284, INSERM U1081, IRCAN, Nice, France.
The British journal of dermatology.Br J Dermatol.2013 Apr;168(4):808-814. doi: 10.1111/bjd.12202.
Background Genetic mutations in the plectin gene (PLEC) cause autosomal recessive forms of epidermolysis bullosa simplex (EBS) associated with either muscular dystrophy (EBS-MD) or pyloric atresia (EBS-PA). Phenotype-genotype analysis has suggested that EBS-MD is due mostly to genetic mutations a
PMID 23289980

Genetics of slaughter precocity, carcass weight and carcass weight gain in Chianina, Marchigiana and Romagnola young bulls under protected geographical indication.

Sbarra F, Mantovani R, Quaglia A, Bittante G.SourceNational Breeders Association of Italian Beef Breeds (ANABIC), Via Visciolosa, 06132 S. Martino in Colle, (PG), Italy.
Journal of animal science.J Anim Sci.2013 Mar 21. [Epub ahead of print]
The aim of this study was i) to estimate the heritability and genetic correlation of the age at slaughter (AS), as an indicator of slaughter precocity, carcass weight (CW) and carcass weight gain (CWG=CW×AS-1) obtained from young bulls of three Italian autochthonous beef cattle breeds, i.e., Chiani
PMID 23519731

Ramieri V, Basile E, Cascone NC, Arangio P, Ungari C, Gennaro P, Di Cataldo A, Sementa A, Romeo MG, Clerico A, La Spina M, D'Amico S, Licciardello M, Milone P, Cascone P.SourceFrom the *Unit of Maxillo-Facial Surgery, Universitá "Sapienza" I Facoltá di Medicina e Chirurgia; and †Unit of Ophthalmology, Universitá "Sapienza" di Roma II Facoltá di Medicina e Chirurgia, Roma; ‡Unit of Pediatric Hematology and Oncology, Universitá di Catania, Catania; §Unit of Pathology, Gaslini Institute, Genoa; ∥Unit of Neonatal Intensive Care, Universitá di Catania, Catania; #Unit of Pediatric Hematology and Oncology, Universitá"Sapienza" I Facoltá di Medicina e Chirurgia, Roma; and ¶Unit of Radiology, Universitá di Catania, Catania, Italy.
The Journal of craniofacial surgery.J Craniofac Surg.2013 Mar;24(2):523-525.
BACKGROUND: Malignant rhabdoid tumors are rare and aggressive tumors of pediatric age. The primary tumor can occur in different localizations, but it mainly involves kidney, soft tissue, or central nervous system. It has been associated to a poor diagnosis.METHODS: The authors present the case of a
PMID 23524732

KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect

Ko Jung Min,Lee Hyo Sung,Hwang Jin Soon
Endocrine Journal 57(8), 701-709, 2010
… Mutations in the GPR54 gene have already been identified as a cause of idiopathic hypogonadotrophic hypogonadism and central precocious puberty (CPP) in certain patients. … This polymorphism was suggested to exert a protective effect on pubertal precocity, even though more evidence will be required to confirm the accurate function. …
NAID 130004443636

Yoshimura Kazuko,Naiki Yasuhiro,Horikawa Reiko,Tanaka Toshiaki
Clinical Pediatric Endocrinology 14(Supplement24), S24_55-S24_57, 2005
… One patient was diagnosed as having central precocious puberty according to the diagnostic guidelines. … The other two patients were on borderline sexual precocity. …
NAID 130004430967