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European Journal of Pediatrics

Volumn 161, Issue 3, 2002, Pages 157-160

Congenital hemihypertrophy and pheochromocytoma, not a coincidental combination?

(4) Van den Akker, Erica L a De Krijger, Ronald R b De Herder, Wouter W b Drop, Stenvert L a

a SOPHIA CHILDREN S HOSPITAL (Netherlands)

b ERASMUS MEDICAL CENTER (Netherlands)

Author keywords

Congenital hemihypertrophy; Pheochromocytoma

Indexed keywords

ADRENALIN; CATECHOLAMINE; DOPAMINE; NORADRENALIN; PHENOXYBENZAMINE; PROPRANOLOL; RENIN; VANILMANDELIC ACID;

ABDOMINAL TUMOR; ADRENAL GLAND; ADULT; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CATECHOLAMINE BLOOD LEVEL; CATECHOLAMINE URINE LEVEL; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; GENE MUTATION; HEMIHYPERTROPHY; HISTOPATHOLOGY; HUMAN; NEUROLOGIC EXAMINATION; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; SCREENING; SYMPTOM;

ADRENAL CORTEX NEOPLASMS; ADRENAL GLANDS; ADULT; BECKWITH-WIEDEMANN SYNDROME; CATECHOLAMINES; FEMALE; HUMANS; HYPERTROPHY; PHEOCHROMOCYTOMA;

EID: 0036180963 PISSN: 03406199 EISSN: None Source Type: Journal
DOI: 10.1007/s00431-001-0901-9 Document Type: Article

Times cited : (10)

References (13)

1
- 0032476038
- Clinical diCerentiation between Proteus syndrome and hemihyperplasia: Description of a distinct form of hemihyperplasia
- (1998) Am J Med Genet , vol.79 , pp. 311-318
- Biesecker, L.G.¹ Peters, K.F.² Darling, T.N.³ Choyke, P.⁴ Hill, S.⁵ Schimke, N.⁶ Cunningham, M.⁷ Meltzer, P.⁸ Cohen, M.M.⁹

2
- 0004062125
- Blackwell, Oxford
- (1990) Birth defects encyclopaedia
- Buyse, M.¹

3
- 17744374251
- Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes
- (2001) J Clin Endocrinol Metab , vol.86 , pp. 1999-2008
- Eisenhofer, G.¹ Walther, M.M.² Huynh, T.T.³ Li, S.T.⁴ Bornstein, S.R.⁵ Vortmeyer, A.⁶ Mannelli, M.⁷ Goldstein, D.S.⁸ Linehan, W.N.⁹ Lenders, J.W.¹⁰ Pacak, K.¹¹

4
- 0028124711
- Clinical features and natural history of Beckwith-Wiedemann syndrome: Presentation of 74 new cases
- (1994) Clin Genet , vol.46 , pp. 168-174
- Elliott, M.¹ Bayly, R.² Cole, T.³ Temple, I.K.⁴ Maher, E.R.⁵

5
- 0032475876
- Isolated hemihyperplasia (hemihypertrophy): Report of a prospective mulitcenter study of the incidence of neoplasia and review
- (1998) Am J Med Genet , vol.79 , pp. 274-278
- Hoyme, H.¹ Seaver, L.H.² Jones, K.L.³ Procopio, F.⁴ Crooks, W.⁵ Feingold, M.⁶

6
- 0024453106
- A genetic study of von Recklinghausen neurofibromatosis in South East Wales. Guidelines for genetic counselling
- (1998) J Med Genet , vol.26 , pp. 712-721
- Huson, S.¹ Compston, D.A.² Harper, P.S.³

7
- 0035293279
- Genetic aspects of pheochromocytoma
- (2001) Endocr Regul , vol.35 , pp. 43-52
- Koch, C.A.¹ Vortmeyer, A.O.² Huang, S.C.³ Alesci, S.⁴ Zhuang, Z.⁵ Pacak, K.⁶

8
- 0017064680
- Congenital hemihypertrophy and malignant giant pheochromocytoma-a previously undescribed coincidence
- (1976) Eur J Pediatr , vol.122 , pp. 263-273
- Schnakenburg, K.V.¹ Muller, M.² Dorner, K.³ Harms, D.⁴ Schwarze, E.W.⁵

9
- 0028034439
- Analysis of paediatric tumour types associated with hemihyperplasia in childhood
- (1994) J Paediatr Child Health , vol.30 , pp. 515-517
- Smith, P.J.¹ Sullivan, M.² Algar, E.³ Shapiro, D.N.⁴

10
- 2642668463
- Germline mutations in the vhl gene in patients presenting with phaeochromocytomas
- (1998) Int J Cancer , vol.77 , pp. 337-340
- Van der Harst, E.¹ De Krijger, R.R.² Dinjens, W.N.³ Weeks, L.E.⁴ Bonjer, H.J.⁵ Bruining, H.A.⁶ Lamberts, S.W.⁷ Koper, J.W.⁸

11
- 0037896855
- 111In-octreotide uptake in benign and malignant pheochromocytomas
- (2001) J Clin Endocrinol Metab , vol.86 , pp. 685-693
- Van der Harst, E.¹ De Herder, W.W.² Bruining, H.A.³ Bonjer, H.J.⁴ De Krijger, R.R.⁵ Lamberts, S.W.J.⁶ Van de Meiracker, A.H.⁷ Boomsma, F.⁸ Stijnen, T.⁹ Krenning, E.P.¹⁰ Bosman, F.T.¹¹ Kwekkeboom, D.J.¹²

12
- 0031031959
- Frequency of Wiedemann-Beckwith syndrome in Germany; rate of hemihyperplasia and of tumours in affected children
- (1997) Eur J Pediatr , vol.156 , pp. 251
- Wiedemann, H.R.¹

13
- 0034701247
- Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis
- (2000) Hum Mol Genet , vol.9 , pp. 765-768
- Zhou, X.P.¹ Marsh, D.J.² Hampel, H.³ Mulliken, J.B.⁴ Gimm, O.⁵ Eng, C.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.