Literature DB >> 14259270

A-BETA-LIPOPROTEINAEMIA (BASSEN-KORNZWEIG SYNDROME): REPORT OF A CASE.

D M BECROFT, J M COSTELLO, P J SCOTT.   

Abstract

Keywords:  ABETALIPOPROTEINEMIA; AMINOACIDURIA, RENAL; BLOOD CHOLESTEROL; CONSANGUINITY; DIAGNOSIS, DIFFERENTIAL; ETHNOLOGY; HEART FAILURE, CONGESTIVE; INFANT; KIDNEY FUNCTION TESTS; LIPID METABOLISM; LIPID METABOLISM, INBORN ERRORS; LIPOPROTEINS; LUNG DISEASES; NEW ZEALAND; PULMONARY EDEMA; RESPIRATORY TRACT INFECTIONS; SPRUE

Mesh：

Substances：

Year:  1965        PMID： 14259270      PMCID： PMC2019261          DOI： 10.1136/adc.40.209.40

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  27 in total

1.  ACQUIRED ACANTHOCYTOSIS AND MYELOPHTHISIS IN A CASE OF EALES'S DISEASE.

Authors:  A KAHAN; I L KAHAN; A BENKO
Journal:  Br J Ophthalmol       Date:  1963-10       Impact factor: 4.638

2.  RED-CELL AND PLASMA LIPIDS IN ACANTHOCYTOSIS.

Authors:  P WAYS; C F REED; D J HANAHAN
Journal:  J Clin Invest       Date:  1963-08       Impact factor: 14.808

3.  A human lipoprotein polymorphism.

Authors:  B S BLUMBERG; D BERNANKE; A C ALLISON
Journal:  J Clin Invest       Date:  1962-10       Impact factor: 14.808

4.  Infantile pyknocytosis occurring in dissimilar twins.

Authors:  V A LOVRIC
Journal:  Med J Aust       Date:  1960-10-08       Impact factor: 7.738

5.  [The congenital absence of beta-lipoproteins].

Authors:  M LAMY; J FREZAL; J POLONOVSKI; J REY
Journal:  Presse Med       Date:  1961-07-08       Impact factor: 1.228

6.  Hypocholesteremia in idiopathic steatorrhea with report of a case of profound hypocholesteremia of lifelong standing.

Authors:  I S FRIEDMAN; H COHN; M ZYMARIS; M G GOLDNER
Journal:  Arch Intern Med       Date:  1960-01

7.  Retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease.

Authors:  A L KORNZWEIG; F A BASSEN
Journal:  AMA Arch Ophthalmol       Date:  1957-08

8.  The burr red cell and azotaemia.

Authors:  W A AHERNE
Journal:  J Clin Pathol       Date:  1957-08       Impact factor: 3.411

9.  Atypical retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease.

Authors:  R S JAMPEL; H F FALLS
Journal:  AMA Arch Ophthalmol       Date:  1958-06

10.  An unusual syndrome of hemolytic anemia, thrombocytopenic purpura and renal disease.

Authors:  C N SHUMWAY; G MILLER
Journal:  Blood       Date:  1957-12       Impact factor: 22.113
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  1 in total

1.  Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function.

Authors:  Sebastian Zeissig; Stephanie K Dougan; Duarte C Barral; Yvonne Junker; Zhangguo Chen; Arthur Kaser; Madelyn Ho; Hannah Mandel; Adam McIntyre; Susan M Kennedy; Gavin F Painter; Natacha Veerapen; Gurdyal S Besra; Vincenzo Cerundolo; Simon Yue; Sarah Beladi; Samuel M Behar; Xiuxu Chen; Jenny E Gumperz; Karine Breckpot; Anna Raper; Amanda Baer; Mark A Exley; Robert A Hegele; Marina Cuchel; Daniel J Rader; Nicholas O Davidson; Richard S Blumberg
Journal:  J Clin Invest       Date:  2010-07-01       Impact factor: 14.808
  1 in total

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