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2. Autosomal recessive form of connatal Pelizaeus-Merzbacher disease. Begleiter ML; Harris DJ Am J Med Genet; 1989 Jul; 33(3):311-3. PubMed ID: 2679088 [TBL] [Abstract][Full Text] [Related]
3. [Female autopsy case of Seitelberger's connatal form of Pelizaeus-Merzbacher disease]. Shimizu Y; Shioda K; Takada K; Minagawa M; Isshiki T No To Hattatsu; 1997 Nov; 29(6):507-13. PubMed ID: 9394608 [TBL] [Abstract][Full Text] [Related]
4. Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms. Wang PJ; Young C; Liu HM; Chang YC; Shen YZ Pediatr Neurol; 1995 Jan; 12(1):47-53. PubMed ID: 7748360 [TBL] [Abstract][Full Text] [Related]
5. Connatal Pelizaeus-Merzbacher disease associated with the jimpy(msd) mice mutation. Komaki H; Sasaki M; Yamamoto T; Iai M; Takashima S Pediatr Neurol; 1999 Apr; 20(4):309-11. PubMed ID: 10328282 [TBL] [Abstract][Full Text] [Related]
6. Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins. Renier WO; Gabreëls FJ; Hustinx TW; Jaspar HH; Geelen JA; Van Haelst UJ; Lommen EJ; Ter Haar BG Acta Neuropathol; 1981; 54(1):11-7. PubMed ID: 7234326 [TBL] [Abstract][Full Text] [Related]
7. Pelizaeus-Merzbacher disease: classical or connatal? Scheffer IE; Baraitser M; Wilson J; Harding B; Kendall B; Brett EM Neuropediatrics; 1991 May; 22(2):71-8. PubMed ID: 1857497 [TBL] [Abstract][Full Text] [Related]
9. Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein. Gencic S; Abuelo D; Ambler M; Hudson LD Am J Hum Genet; 1989 Sep; 45(3):435-42. PubMed ID: 2773936 [TBL] [Abstract][Full Text] [Related]
10. Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings. Ulrich J; Herschkowitz N Acta Neuropathol; 1977 Oct; 40(2):129-36. PubMed ID: 201145 [TBL] [Abstract][Full Text] [Related]
11. Occidental type cerebromuscular dystrophy: a report of eleven cases. Topaloğlu H; Yalaz K; Renda Y; Cağlar M; Göğüs S; Kale G; Gücüyener K; Nurlu G J Neurol Neurosurg Psychiatry; 1991 Mar; 54(3):226-9. PubMed ID: 2030350 [TBL] [Abstract][Full Text] [Related]
12. A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene. Harding B; Ellis D; Malcolm S Neuropathol Appl Neurobiol; 1995 Apr; 21(2):111-5. PubMed ID: 7541900 [TBL] [Abstract][Full Text] [Related]
13. Pelizaeus-Merzbacher disease in a brother and sister. Pamphlett R; Silberstein P Acta Neuropathol; 1986; 69(3-4):343-6. PubMed ID: 3962612 [TBL] [Abstract][Full Text] [Related]
14. Arthrogryposis associated with connatal Pelizaeus-Merzbacher disease: case report. Novotny EJ Neuropediatrics; 1988 Nov; 19(4):221-3. PubMed ID: 3205380 [TBL] [Abstract][Full Text] [Related]
15. The reflection of histology in MR imaging of Pelizaeus-Merzbacher disease. van der Knaap MS; Valk J AJNR Am J Neuroradiol; 1989; 10(1):99-103. PubMed ID: 2492735 [TBL] [Abstract][Full Text] [Related]
16. Connatal Pelizaeus-Merzbacher disease in two girls. Ziereisen F; Dan B; Christiaens F; Deltenre P; Boutemy R; Christophe C Pediatr Radiol; 2000 Jul; 30(7):435-8. PubMed ID: 10929359 [TBL] [Abstract][Full Text] [Related]
17. [Connatal type of Pelizaeus-Merzbacher disease: a case report]. Kagitani K; Fukunishi M; Mano T; Matsuoka T; Imai K; Ono J; Okada S No To Hattatsu; 1999 Mar; 31(2):171-6. PubMed ID: 10191641 [TBL] [Abstract][Full Text] [Related]
19. Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein (PLP) gene. Pratt VM; Dlouhy SR; Hodes ME Clin Genet; 1995 Feb; 47(2):99-100. PubMed ID: 7541731 [TBL] [Abstract][Full Text] [Related]
20. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease. Koeppen AH; Ronca NA; Greenfield EA; Hans MB Ann Neurol; 1987 Feb; 21(2):159-70. PubMed ID: 3827224 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]