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4. Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families. Pessah M; Benlian P; Beucler I; Loux N; Schmitz J; Junien C; Infante R J Clin Invest; 1991 Jan; 87(1):367-70. PubMed ID: 1985110 [TBL] [Abstract][Full Text] [Related]
5. Using genetically engineered mice to understand apolipoprotein-B deficiency syndromes in humans. Raabe M; Kim E; Véniant M; Nielsen LB; Young SG Proc Assoc Am Physicians; 1998; 110(6):521-30. PubMed ID: 9824535 [TBL] [Abstract][Full Text] [Related]
6. Anderson's disease: no linkage to the apo B locus. Strich D; Goldstein R; Phillips A; Shemer R; Goldberg Y; Razin A; Freier S J Pediatr Gastroenterol Nutr; 1993 Apr; 16(3):257-64. PubMed ID: 8492252 [TBL] [Abstract][Full Text] [Related]
7. Chylomicron retention disease--the role of ultrastructural examination in differential diagnosis. Boldrini R; Biselli R; Bosman C Pathol Res Pract; 2001; 197(11):753-7. PubMed ID: 11770019 [TBL] [Abstract][Full Text] [Related]
8. Receptor-ligand interactions in the hepatic uptake of chylomicron remnants studied with genetically manipulated mice. Redgrave TG; Mortimer BC; Martins IJ Z Gastroenterol; 1996 Jun; 34 Suppl 3():105-7. PubMed ID: 8767480 [No Abstract] [Full Text] [Related]
9. [Anderson's disease (steatorrhea due to the retention of chylomicrons): diagnostic criteria]. Oltra Benavent M; Chirivella Casanova M; Pereda Pérez A; Ribes Konickx C; Ferrer Calvete J An Esp Pediatr; 1997 Aug; 47(2):195-8. PubMed ID: 9382356 [No Abstract] [Full Text] [Related]
12. Apolipoprotein B-48 as a marker for chylomicrons and their remnants: studies in the postprandial state. Isherwood SG; Williams CM; Gould BJ Proc Nutr Soc; 1997 Mar; 56(1B):497-505. PubMed ID: 9168557 [No Abstract] [Full Text] [Related]
13. Mental retardation and ataxia due to normotriglyceridemic hypobetalipoproteinemia. Homer VM; George PM; du Toit S; Davidson JS; Wilson CJ Ann Neurol; 2005 Jul; 58(1):160-3. PubMed ID: 15984016 [TBL] [Abstract][Full Text] [Related]