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H Pihko

Showing results (71-80 of 98) with videos related to

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Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Benign muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Journal of Medical Genetics|November 1, 1987
The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probandsL Keskiaho, S Knuutila, H Pihko, et al.
Muscle & Nerve|January 1, 1993
Progressive unilateral hypertrophic myopathy: a case studyH Pihko, I Lehtinen, H Tikkanen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1997
Improving outcome of malignant brain tumours in very young children: a population-based study in Finland during 1975-93I Ilveskoski, H Pihko, R Sankila, et al.
Journal of Pediatric Orthopedics. Part B|April 1, 1997
Psychosocial development and premorbid skeletal growth in Legg-Calvé-Perthes disease: a study of nineteen patientsT T Lahdes-Vasama, I S Sipilä, S Lamminranta, et al.
Medical and Pediatric Oncology|July 1, 1996
Ototoxicity in children with malignant brain tumors treated with the "8 in 1" chemotherapy protocolI Ilveskoski, U M Saarinen, T Wiklund, et al.
Pediatric Hematology and Oncology|January 1, 1996
Chemotherapy with the "8 in 1" protocol for malignant brain tumors in children: a population-based study in FinlandI Ilveskoski, U M Saarinen, M Perkkiö, et al.
American Journal of Medical Genetics|July 1, 1990
Muscle-eye-brain disease and Walker-Warburg syndromeP Santavuori, H Pihko, K Sainio, et al.
American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Benign muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Journal of Medical Genetics|November 1, 1987
The inheritance of fragile sites: apparent absence of fra(2)(q13) in the parents of three unrelated probandsL Keskiaho, S Knuutila, H Pihko, et al.
Muscle & Nerve|January 1, 1993
Progressive unilateral hypertrophic myopathy: a case studyH Pihko, I Lehtinen, H Tikkanen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1997
Improving outcome of malignant brain tumours in very young children: a population-based study in Finland during 1975-93I Ilveskoski, H Pihko, R Sankila, et al.
Journal of Pediatric Orthopedics. Part B|April 1, 1997
Psychosocial development and premorbid skeletal growth in Legg-Calvé-Perthes disease: a study of nineteen patientsT T Lahdes-Vasama, I S Sipilä, S Lamminranta, et al.
Medical and Pediatric Oncology|July 1, 1996
Ototoxicity in children with malignant brain tumors treated with the "8 in 1" chemotherapy protocolI Ilveskoski, U M Saarinen, T Wiklund, et al.
Pediatric Hematology and Oncology|January 1, 1996
Chemotherapy with the "8 in 1" protocol for malignant brain tumors in children: a population-based study in FinlandI Ilveskoski, U M Saarinen, M Perkkiö, et al.
American Journal of Medical Genetics|July 1, 1990
Muscle-eye-brain disease and Walker-Warburg syndromeP Santavuori, H Pihko, K Sainio, et al.
American Journal of Human Genetics|January 23, 1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mappingB Cormand, K Avela, H Pihko, et al.
Pageof 10