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42. Sjögren-Larsson syndrome: microscopic and scanning electron microscopic findings in replicas of the skin. Jagell S; Hofer PA Acta Derm Venereol; 1982; 62(5):397-400. PubMed ID: 6183888 [TBL] [Abstract][Full Text] [Related]
46. The Sjögren-Larsson syndrome. A case report. Theile U; Jensen M Humangenetik; 1973; 17(2):155-9. PubMed ID: 4691149 [No Abstract] [Full Text] [Related]
47. Sjogren - Larsson Syndrome: a case report. Dhanuka AK; Gupta M Neurol India; 2002 Sep; 50(3):371-2. PubMed ID: 12391475 [TBL] [Abstract][Full Text] [Related]
48. Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities. Devriendt K; van den Oord J; De Vos R; Van den Berghe H; Fryns JP Am J Med Genet; 1996 Jan; 61(2):127-30. PubMed ID: 8669437 [TBL] [Abstract][Full Text] [Related]
50. [Sjögren-Larsson syndrome: a novel mutation in a Moroccan child]. Rafai MA; Boulaajaj FZ; Seito A; Suga Y; Slassi I; Fadel H Arch Pediatr; 2008 Nov; 15(11):1648-51. PubMed ID: 18951768 [TBL] [Abstract][Full Text] [Related]
51. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy. Stoll C; Eyer D Ann Genet; 1999; 42(1):45-50. PubMed ID: 10214507 [TBL] [Abstract][Full Text] [Related]
52. Sjögren-larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients. Gånemo A; Jagell S; Vahlquist A Acta Derm Venereol; 2009; 89(1):68-73. PubMed ID: 19197545 [TBL] [Abstract][Full Text] [Related]
53. A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease). Balci S; Demirçeken FG; Ocal B; Zorlu P; Teziç T Turk J Pediatr; 2001; 43(4):366-8. PubMed ID: 11765173 [TBL] [Abstract][Full Text] [Related]
54. [Genetic counseling in Sjögren-Larsson syndrome (author's transl)]. Theile U Z Orthop Ihre Grenzgeb; 1978; 116(6):912-4. PubMed ID: 726579 [TBL] [Abstract][Full Text] [Related]
55. Zinc and copper concentration in serum of patients with congenital ichthyosis, spastic di- or tetraplegia and mental retardation (Sjögren-Larsson syndrome). Jagell S; Hallmans G; Gustavson KH Ups J Med Sci; 1981; 86(3):291-5. PubMed ID: 7324288 [TBL] [Abstract][Full Text] [Related]
56. Atrichia, ichthyosis, follicular hyperkeratosis, chronic candidiasis, keratitis, seizures, mental retardation and inguinal hernia: a severe manifestation of IFAP syndrome? Boente MC; Bibas-Bonet H; Coronel AM; Asial RA Eur J Dermatol; 2000 Mar; 10(2):98-102. PubMed ID: 10694306 [TBL] [Abstract][Full Text] [Related]
57. [Congenital neuroichthyosis and psychiatric involvement. Apropos of a case]. Donnet A; Samuelian JC Encephale; 1988; 14(6):427-9. PubMed ID: 3068048 [TBL] [Abstract][Full Text] [Related]
58. [Differential diagnosis of autosomal-dominant chthyosis vulgaris and X-chromosome ichthyosis]. Hofbauer M; Schnyder UW Hautarzt; 1974 Jul; 25(7):319-25. PubMed ID: 4409230 [No Abstract] [Full Text] [Related]
59. [Differential diagnosis of ophthalmological findings in various forms of ichthyosis]. Hammerstein W; Haensch R Fortschr Med; 1978 Feb; 96(6):245-51. PubMed ID: 620989 [TBL] [Abstract][Full Text] [Related]
60. Sjögren-Larsson syndrome. (Congenital ichthyosis with spastic paralysis and oligophrenia). Gellis SS; Feingold M Am J Dis Child; 1968 Dec; 116(6):653-4. PubMed ID: 5697194 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]