SCOPUS 정보 검색 플랫폼

Volumn 145, Issue 4, 2004, Pages 567-

A molecular diagnosis of hyperparathyroidism - Jaw tumor syndrome in an adolescent with recurrent kidney stones

(8) Howell, Viive M a Zori, Roberto T b Stalker, Heather J b Williams, Charles b Jesse, Nathan b Nelson, Anne E a Robinson, Bruce G c Marsh, Deborah J d

a UNIVERSITY OF SYDNEY (Australia)

b UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE (United States)

c GARVAN INSTITUTE OF MEDICAL RESEARCH (Australia)

d ROYAL NORTH SHORE HOSPITAL (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ANAMNESIS; ARTICLE; CASE REPORT; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; FAMILY HISTORY; GENE MUTATION; HUMAN; HYPERCALCEMIA; HYPERPARATHYROIDISM; JAW TUMOR; LABORATORY TEST; MALE; NEPHROLITHIASIS; NUCLEOTIDE SEQUENCE; PARATHYROID TUMOR; PATIENT CARE; PRIORITY JOURNAL; RECURRENT DISEASE;

EID: 5144223335 PISSN: 00223476 EISSN: None Source Type: Journal
DOI: 10.1016/j.jpeds.2004.04.023 Document Type: Article

Times cited : (16)

References (4)

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2
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- HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours
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3
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- Familial isolated hyperparathyroidism: Clinical and genetic characteristics of 36 kindreds
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- Simonds, W.F.¹ James-Newton, L.A.² Agarwal, S.K.³ Yang, B.⁴ Skarulis, M.C.⁵ Hendy, G.N.⁶

4
- 0031863057
- Clinical profile of primary hyperparathyroidism in adolescents and young adults
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.