These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
7. [Clinical aspects of hereditary peroxisomal disorders]. Billette de Villemeur T; Poll The BT; Saudubray JM Minerva Pediatr; 1991 Mar; 43(3):115-23. PubMed ID: 1870505 [No Abstract] [Full Text] [Related]
8. [Should a metabolic work-up be performed in autism?]. Schiff M; Delorme R; Benoist JF; Ogier de Baulny H Arch Pediatr; 2010 Jun; 17(6):802-3. PubMed ID: 20654901 [No Abstract] [Full Text] [Related]
9. [Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases]. Jaffray JY; Charbonne F; Rousseau P; Malpuech G; Meyer M; Labbe A; Malet P Pathol Biol (Paris); 1986 Feb; 34(2):91-8. PubMed ID: 3517782 [TBL] [Abstract][Full Text] [Related]
10. [New aspects in diagnosis and therapy of hereditary diseases of the nervous and skeletal systems]. Plecko B; Paschke E Wien Klin Wochenschr; 1997 Feb; 109(3):65-7. PubMed ID: 9139463 [No Abstract] [Full Text] [Related]
11. Diagnosis of neurometabolic disorders by examination of skin biopsies and lymphocytes. Dolman CL Semin Diagn Pathol; 1984 May; 1(2):82-97. PubMed ID: 6100973 [TBL] [Abstract][Full Text] [Related]
12. [Early diagnosis of Lafora disease. Significance of paroxysmal visual manifestations and contribution of skin biopsy]. Roger J; Pellissier JF; Bureau M; Dravet C; Revol M; Tinuper P Rev Neurol (Paris); 1983; 139(2):115-24. PubMed ID: 6410486 [TBL] [Abstract][Full Text] [Related]
14. A case of Lafora's disease: diagnosis by skin biopsy. Yalçiner B; Ozer F; Hanoglu L; Ozkara C; Ozbay G; Arpaci B Acta Neurol Belg; 1993; 93(2):97-8. PubMed ID: 8389505 [No Abstract] [Full Text] [Related]
15. [Skin biopsy: a valuable aid for the diagnosis of rare neurologic disorders]. Corcia P; Martin L Ann Dermatol Venereol; 1999 Oct; 126(10):723-4. PubMed ID: 10604015 [No Abstract] [Full Text] [Related]
16. Ultrastructural examination of the axillary skin biopsy in the diagnosis of metabolic diseases. Abramovich CM; Prayson RA; McMahon JT; Cohen BH Hum Pathol; 2001 Jun; 32(6):649-55. PubMed ID: 11431721 [TBL] [Abstract][Full Text] [Related]
17. Progressive myoclonus epilepsies: specific causes and diagnosis. Berkovic SF; Andermann F; Carpenter S; Wolfe LS N Engl J Med; 1986 Jul; 315(5):296-305. PubMed ID: 3088452 [No Abstract] [Full Text] [Related]
18. [Advances in biochemistry in the understanding of neurometabolic disorders]. Ribes A; Briones P; Rodés M Rev Neurol; 1999 Jan 1-15; 28(1):11-5. PubMed ID: 10101758 [TBL] [Abstract][Full Text] [Related]
19. [Diagnostic procedure in neurodegenerative diseases with a chronic course]. Boltshauser E; Spycher MA Klin Padiatr; 1986; 198(2):79-83. PubMed ID: 3702276 [TBL] [Abstract][Full Text] [Related]