SCOPUS 정보 검색 플랫폼

Volumn 16, Issue 6, 2009, Pages 553-555

Biological diagnosis of red cell membrane disorders;Diagnostic biologique des maladies constitutionnelles de la membrane érythrocytaire

(1) Garcon L a

a HÔTEL DIEU (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CYTOMETRY; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; ELECTROPHORESIS; ERYTHROCYTE DISORDER; ERYTHROCYTE MEMBRANE; HEREDITARY SPHEROCYTOSIS; HUMAN; MEMBRANE PERMEABILITY; SCREENING TEST;

CHILD; ERYTHROCYTES, ABNORMAL; HEMATOLOGIC DISEASES; HUMANS;

EID: 67149127031 PISSN: 0929693X EISSN: None Source Type: Journal
DOI: 10.1016/S0929-693X(09)74064-3 Document Type: Article

Times cited : (3)

References (8)

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2
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- Disorders of red cell membrane
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3
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- Sphérocytose héréditaire : recommandations pour le diagnostic et la prise en charge chez l'enfant
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- Guitton, G.¹ Garçon, L.² Cynober, T.³

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- Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity
- Cynober T., Mohandas N., and Tchernia G. Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. J Lab Clin Med 128 (1996) 259-266
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- Cynober, T.¹ Mohandas, N.² Tchernia, G.³

5
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- Usefulness of the eosin-5'-maleimid cytometric method as a first line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis
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6
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- The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations
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7
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- Thrombo-embolic disease after splenectomy for hereditary stomatocytosis
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8
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- A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.