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3. Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalities. Pierquin G; Peeters P; Roels F; Vamos E; Brucher JM; Tint GS; Honda A; Van Regemorter N Am J Med Genet; 1995 Apr; 56(3):276-80. PubMed ID: 7778589 [TBL] [Abstract][Full Text] [Related]
4. [Contribution to the cerebrohepatorenal syndrome]. Fehlow P Padiatr Grenzgeb; 1986; 25(4):337-41. PubMed ID: 3774333 [No Abstract] [Full Text] [Related]
5. [The so-called lipophanerosis of the globus pallidus]. Borrone C; Bugiani O; De Negri M; Durand P; Mastropaolo C Acta Neurol (Napoli); 1969; 24(2):238-47. PubMed ID: 5386343 [No Abstract] [Full Text] [Related]
6. Clinical phenotype of desmosterolosis. FitzPatrick DR; Keeling JW; Evans MJ; Kan AE; Bell JE; Porteous ME; Mills K; Winter RM; Clayton PT Am J Med Genet; 1998 Jan; 75(2):145-52. PubMed ID: 9450875 [TBL] [Abstract][Full Text] [Related]
7. [Disorders of neuronal migration in Zellwegers cerebrohepato-renal syndrome (author's transl)]. Garzuly F; Szabo L; Kadas L Neuropadiatrie; 1974 Aug; 5(3):318-28. PubMed ID: 4479896 [No Abstract] [Full Text] [Related]
8. [Diagnosis of Zellweger's cerebrohepatorenal syndrome]. Schutgens RB; Heymans HS; Purvis R; Wanders RJ; Schrakamp G; van den Bosch H Tijdschr Kindergeneeskd; 1984 Dec; 52(6):231-8. PubMed ID: 6528320 [TBL] [Abstract][Full Text] [Related]
9. Unusual case of Smith-Lemli-Opitz syndrome "type II". Seller MJ; Russell J; Tint GS Am J Med Genet; 1995 Apr; 56(3):265-8. PubMed ID: 7778586 [TBL] [Abstract][Full Text] [Related]
10. The cerebro-hepato-renal (Zellweger) syndrome and other peroxisomal disorders. Zellweger H Dev Med Child Neurol; 1987 Dec; 29(6):821-9. PubMed ID: 3319743 [No Abstract] [Full Text] [Related]
15. Review: the cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects. Kelley RI Am J Med Genet; 1983 Dec; 16(4):503-17. PubMed ID: 6362411 [TBL] [Abstract][Full Text] [Related]
16. Neonatal cholestatic syndromes associated with alterations in bile acid synthesis. Freese DK; Hanson RF J Pediatr Gastroenterol Nutr; 1983 May; 2(2):374-80. PubMed ID: 6348235 [TBL] [Abstract][Full Text] [Related]
17. Fatty acid oxidation disorder as a cause of sudden infant death syndrome (SIDS)--a case report. Thanka J; Padmasani ; Krishnan L; Kuruvilla S Indian J Pathol Microbiol; 2005 Oct; 48(4):485-7. PubMed ID: 16366103 [TBL] [Abstract][Full Text] [Related]
18. The renal lesion in syndromes of multiple congenital malformations. Cerebrohepatorenal syndrome; Jeune asphyxiating thoracic dystrophy; tuberous sclerosis; Meckel syndrome. Bernstein J; Brough AJ; McAdams AJ Birth Defects Orig Artic Ser; 1974; 10(4):35-43. PubMed ID: 4470905 [TBL] [Abstract][Full Text] [Related]
20. Fatal familial steatosis of the liver and kidney in two siblings. Räsänen O; Korhonen M; Similä S; Autere T; Hakosalo J Z Kinderheilkd; 1971; 110(4):267-75. PubMed ID: 5567005 [No Abstract] [Full Text] [Related] [Next] [New Search]