Pihko H - Search Results

1

Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic.

Ranta S, Pihko H, Santavuori P, Tahvanainen E, de la Chapelle A. Ranta S, et al. Among authors: pihko h. Neuromuscul Disord. 1995 May;5(3):221-5. doi: 10.1016/0960-8966(94)00058-h. Neuromuscul Disord. 1995. PMID: 7633187

2

Ocular findings in muscle-eye-brain (MEB) disease: a follow-up study.

Pihko H, Lappi M, Raitta C, Sainio K, Valanne L, Somer H, Santavuori P. Pihko H, et al. Brain Dev. 1995 Jan-Feb;17(1):57-61. doi: 10.1016/0387-7604(94)00101-3. Brain Dev. 1995. PMID: 7762765

3

MRI of the brain in muscle-eye-brain (MEB) disease.

Valanne L, Pihko H, Katevuo K, Karttunen P, Somer H, Santavuori P. Valanne L, et al. Among authors: pihko h. Neuroradiology. 1994 Aug;36(6):473-6. doi: 10.1007/BF00593687. Neuroradiology. 1994. PMID: 7991095

4

Muscle-eye-brain disease: a neuropathological study.

Haltia M, Leivo I, Somer H, Pihko H, Paetau A, Kivelä T, Tarkkanen A, Tomé F, Engvall E, Santavuori P. Haltia M, et al. Among authors: pihko h. Ann Neurol. 1997 Feb;41(2):173-80. doi: 10.1002/ana.410410208. Ann Neurol. 1997. PMID: 9029066

5

Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.

Cormand B, Avela K, Pihko H, Santavuori P, Talim B, Topaloglu H, de la Chapelle A, Lehesjoki AE. Cormand B, et al. Among authors: pihko h. Am J Hum Genet. 1999 Jan;64(1):126-35. doi: 10.1086/302206. Am J Hum Genet. 1999. PMID: 9915951 Free PMC article.

6

Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.

Auranen M, Rapola J, Pihko H, Haltia M, Leivo I, Soinila S, Virtanen I, Kalimo H, Anderson LV, Santavuori P, Somer H. Auranen M, et al. Among authors: pihko h. Neuromuscul Disord. 2000 Jan;10(1):16-23. doi: 10.1016/s0960-8966(99)00066-8. Neuromuscul Disord. 2000. PMID: 10677859

7

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.

Cormand B, Pihko H, Bayés M, Valanne L, Santavuori P, Talim B, Gershoni-Baruch R, Ahmad A, van Bokhoven H, Brunner HG, Voit T, Topaloglu H, Dobyns WB, Lehesjoki AE. Cormand B, et al. Among authors: pihko h. Neurology. 2001 Apr 24;56(8):1059-69. doi: 10.1212/wnl.56.8.1059. Neurology. 2001. PMID: 11320179

8

Muscle-eye-brain disease: clinical features, visual evoked potentials and brain imaging in 20 patients.

Santavuori P, Valanne L, Autti T, Haltia M, Pihko H, Sainio K. Santavuori P, et al. Among authors: pihko h. Eur J Paediatr Neurol. 1998;2(1):41-7. doi: 10.1016/1090-3798(98)01004-1. Eur J Paediatr Neurol. 1998. PMID: 10726845

9

Palmitate oxidation in muscle mitochondria of patients with the juvenile form of neuronal ceroid-lipofuscinosis.

Majander A, Pihko H, Santavuori P. Majander A, et al. Among authors: pihko h. Am J Med Genet. 1995 Jun 5;57(2):298-300. doi: 10.1002/ajmg.1320570237. Am J Med Genet. 1995. PMID: 7668349

10

Benign muscular dystrophy with autosomal dominant inheritance.

Somer H, Laulumaa V, Paljärvi L, Partanen J, Lamminen A, Pihko H, Sariola H, Haltia M. Somer H, et al. Among authors: pihko h. Neuromuscul Disord. 1991;1(4):267-73. doi: 10.1016/0960-8966(91)90100-7. Neuromuscul Disord. 1991. PMID: 1822805

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