7 HEREDITARY SYNDROMES WITH PIGMENTARY RETINOPATHY - A REVIEW AND DIFFERENTIAL-DIAGNOSIS

被引：11

作者：

CANTANI, A

BELLIONI, P

BAMONTE, G

SALVINELLI, F

BAMONTE, MT

机构：

[1] UNIV CATTOLICA SACRO CUORE, DEPT OTORHINOLARYNGOL, I-00168 ROME, ITALY

[2] UNIV ROMA LA SAPIENZA, DEPT OPHTHALMOLOGY, I-00161 ROMA, ITALY

[3] PEDIAT HOSP BAMBINO GESU, DIV OPHTHALMOL, ROMA, ITALY

来源：

CLINICAL PEDIATRICS | 1985年 / 24卷 / 10期

关键词：

D O I：

10.1177/000992288502401006

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：578 / 583

页数：6

共 35 条

[1]

ALSTROM C H, 1959, Acta Psychiatr Neurol Scand Suppl, V129, P1

[2]

ALSTROM CH, 1979, BIRTH DEFECTS COMPEN, P69

[3]

Bardet G., 1920, THESIS PARIS, V170, P107

[4]

BHATTACHARYA S P, 1945, Indian J Pediatr, V12, P51, DOI 10.1007/BF02818040

[5]

Biedl A., 1922, DEUT MED WOCHENSCHR, V48, P1630

[6]

BIEMOND A, 1934, NED TIJDSCHR GENEES, V78, P1801

[7]

CAGIANUT B, 1977, SCHWEIZ MED WSCHR, V107, P446

[8] OCULAR AND SYSTEMIC MANIFESTATIONS OF THE BARDET-BIEDL SYNDROME [J].

CAMPO, RV ;

AABERG, TM .

AMERICAN JOURNAL OF OPHTHALMOLOGY, 1982, 94 (06) :750-756

[9]

CANTANI A, 1984, AGGIORN PEDIATR, V35, P15

[10] LAURENCE-MOON-BIEDL SYNDROME - REPORT OF AN UNUSUAL FAMILY [J].

CICCARELLI, E ;

VESELL, ES .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1961, 101 (04) :519-+

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