Familial isolated primary hyperparathyroidism - A multiple endocrine neoplasia type 1 variant?

European Journal of Endocrinology

Volumn 145, Issue 2, 2001, Pages 155-160

  Miedlich, S ^a   Lohmann, T ^a   Schneyer, U ^a   Lamesch, P ^a   Paschke, R ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

5 HYDROXYINDOLEACETIC ACID; ALDOSTERONE; CALCIUM; CORTICOTROPIN; DNA; GASTRIN; GLUCAGON; GLUCOSE; GLUTAMINE; HYDROCORTISONE; INSULIN; PARATHYROID HORMONE; PHOSPHATE; POTASSIUM; PROLACTIN; RENIN; SOMATOMEDIN C;

ADOLESCENT; ADULT; ARTICLE; CALCIUM BLOOD LEVEL; CLINICAL ARTICLE; COMPARATIVE STUDY; ENDOCRINE DISEASE; ENDOCRINE GLAND; EXON; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENOTYPE; HUMAN; HYPERCALCEMIA; MALE; MISSENSE MUTATION; MULTIPLE ENDOCRINE NEOPLASIA; PARATHYROID ADENOMA; PARATHYROID HORMONE BLOOD LEVEL; PHENOTYPE; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; SCHOOL CHILD; SCREENING; STATISTICAL ANALYSIS; SYMPTOM;

EID: 0034904731     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1450155     Document Type: Article

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