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13. Familial hypercholesterolemia (Type IIb) in a child: a case report with interesting features. Prasad PV; Chidambaram N Int J Dermatol; 2004 Mar; 43(3):173-5. PubMed ID: 15009385 [TBL] [Abstract][Full Text] [Related]
14. Homozygous familial hypercholesterolaemia presenting with cutaneous xanthomas: response to liver transplantation. Moyle M; Tate B Australas J Dermatol; 2004 Nov; 45(4):226-8. PubMed ID: 15527434 [TBL] [Abstract][Full Text] [Related]
15. Plasma exchange for homozygous familial hypercholesterolaemia: the Cape Town experience. Marais AD; Wood L; Firth JC; Hall JM; Jacobs P Transfus Sci; 1993 Jul; 14(3):239-47. PubMed ID: 10146335 [TBL] [Abstract][Full Text] [Related]
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18. Clinical evaluation of three types of plasmapheresis in a patient with type IIa familial hypercholesterolemia. Mimori A; Takahashi K; Mitamura T; Kato H; Teramoto T; Komuro I; Honda Z; Toma S; Miyamoto T J Clin Apher; 1987; 3(4):209-15. PubMed ID: 3680192 [TBL] [Abstract][Full Text] [Related]
19. LDL-apheresis: clinical experience and indications in the treatment of severe hypercholesterolemia. Thiery J; Seidel D Transfus Sci; 1993 Jul; 14(3):249-59. PubMed ID: 10146336 [TBL] [Abstract][Full Text] [Related]
20. Pinpoint skin lesions in a familial hypercholesterolaemia homozygote. Milionis HJ; Miltiadous GA; Cariolou M; Elisaf MS Acta Paediatr; 2003 Sep; 92(9):1109-10. PubMed ID: 14599079 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]