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1

Progressive unilateral hypertrophic myopathy: A case study

Dr. Helena Pihko, Dr. Ilkka Lehtinen, Dr. Heikki Tikkanen, Dr. Matti Härkönen, Dr. Juhani Rapola, Antti Lamminen, Antero Sahlman, Hannu Somer

Journal:

Year:

1993

Language:

english

File:

PDF, 581 KB

english, 1993

2

Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy

Dr., MD Pekka T. Nokelainen, Dr. Leena Alanen-Kurki, Dr., MD, PhD Hannu V. K. Somer, Dr., MD, PhD S. Helena Pihko, Dr., Md, PhD Leena Peltonen

Journal:

Year:

1991

Language:

english

File:

PDF, 501 KB

english, 1991

3

Muscular dystrophy with separate clinical phenotypes in a large family

Dr., MD Bjarne Udd, Dr., MD, PhD Helena Kääriänen, Dr., MD, Phd Hannu Somer

Journal:

Year:

1991

Language:

english

File:

PDF, 1.02 MB

english, 1991

4

Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study

Petri Luoma, Atle Melberg, Juha O Rinne, Jyrki A Kaukonen, Nina N Nupponen, Richard M Chalmers, Anders Oldfors, Ilkka Rautakorpi, Leena Peltonen, Kari Majamaa, Hannu Somer, Anu Suomalainen

Journal:

Year:

2004

Language:

english

File:

PDF, 470 KB

english, 2004

5

Muscle-eye-brain disease and Walker-Warburg syndrome

Pirkko Santavuori, Helena Pihko, Kimmo Sainio, Marjatta Lappi, Hannu Somer, Matti Haltia, Christina Raitta, Leena Ketonen, Jaakko Leisti

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 140 KB

english, 1990

6

Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease

Dr. Elina Ikonen, Armi Salo, Mirja Somer, Hannu Somer, Leena Pääkkönen, Leena Peltonen

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 597 KB

english, 1992

7

Neuronal intranuclear inclusion disease in identical twins

Dr. Matti Haltia, Hannu Somer, Jorma Palo, William G. Johnson

Journal:

Annals of Neurology

Year:

1984

Language:

english

File:

PDF, 1.67 MB

english, 1984

8

Reply

Matti Haltia, Hannu Somer, Jorma Palo

Journal:

Annals of Neurology

Year:

1985

Language:

english

File:

PDF, 219 KB

english, 1985

9

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population

Pekka Nokelainen, Leena Alanen-Kurki, Robert Winqvist, Björn Falck, Hannu Somer, Jaakko Leisti, Keith Johnson, Marja-Liisa Savontaus, Leena Peltonen

Journal:

Year:

1990

Language:

english

File:

PDF, 476 KB

english, 1990

10

Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2)

Hanna Harno, Timo Hirvonen, MariA. Kaunisto, Heikki Aalto, Hilla Levo, Elina Isotalo, Hannu Somer, Mikko Kallela, Aarno Palotie, Maija Wessman, Markus Färkkilä

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 3.49 MB

english, 2004

11

Abnormal blood lactate accumulation after exercise in patients with multiple mitochondrial DNA deletions and minor muscular symptoms

Harri Lindholm, Mervi Löfberg, Hannu Somer, Hannu Näveri, Anssi Sovijärvi

Journal:

Clinical Physiology and Functional Imaging

Year:

2004

Language:

english

File:

PDF, 90 KB

english, 2004

12

10.1038/13383

Hutton, Mike, Prihar, Guy, Verkkoniem, Auli, Perez-Tur, Jordi, Crook, Richard, Lincoln, Sarah, Houlden, Henry, Somer, Mirja, Paetau, Anders, Kalimo, Hannu, Grover, Andrew, Myllykangas, Liisa, Hardy, J

Journal:

Nature Medicine

Year:

1999

Language:

english

File:

PDF, 114 KB

english, 1999

13

Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies

Michele, Daniel E., Barresi, Rita, Kanagawa, Motoi, Saito, Fumiaki, Cohn, Ronald D., Satz, Jakob S., Dollar, James, Nishino, Ichizo, Kelley, Richard I., Somer, Hannu

Journal:

Year:

2002

Language:

english

File:

PDF, 503 KB

english, 2002

14

An autosomal locus predisposing to deletions of mitochondrial DNA

Suomalainen, Anu, Kaukonen, Jyrki, Amati, Patrizia, Timonen, Ritva, Haltia, Matti, Weissenbach, Jean, Zeviani, Massimo, Somer, Hannu, Peltonen, Leena

Journal:

Nature Genetics

Year:

1995

File:

PDF, 671 KB

1995

15

Morbid Obesity, Gastric Plication and a Severe Neurological Deficit

HANNU SOMER, LEA BERGSTRÖM, PERTTI MUSTAJOKI, LIISA ROVAMO

Journal:

Journal of Internal Medicine

Year:

1985

Language:

english

File:

PDF, 143 KB

english, 1985

16

Neuronal intranuclear inclusion disease : Clinical ophthalmological features and ophthalmic pathology

Matti Haltia, Ahti Tarkkanen, Hannu Somer, Jorma Palo, Hillevi Karli

Journal:

Acta Ophthalmologica (Blackwell)

Year:

1986

Language:

english

File:

PDF, 1.53 MB

english, 1986

17

Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance

Hannu Somer, Arja Voutilainen, Sakari Knuutila, Ilkka Kaitila, Juhani Rapola, Hannu Leinonen

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 422 KB

english, 1985

18

Determination of serum creatine kinase isoenzymes in myocardial infarction

Aarne Konttinen, Hannu Somer

Journal:

The American Journal of Cardiology

Year:

1972

Language:

english

File:

PDF, 500 KB

english, 1972

19

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

Matti Haltia, Frances Prelli, Jorge Ghiso, Sari Kiuru, Hannu Somer, Jorma Palo, Blas Frangione

Journal:

Biochemical and Biophysical Research Communications

Year:

1990

Language:

english

File:

PDF, 1.31 MB

english, 1990

20

A method allowing the quantitation of serum creatine kinase isoenzymes

Hannu Somer, Aarne Konttinen

Journal:

Clinica Chimica Acta

Year:

1972

Language:

english

File:

PDF, 696 KB

english, 1972

21

An electrophoretic method for the quantitation of aspartate aminotransferase isoenzymes

Juhani Murros, Aarne Konttinen, Hannu Somer

Journal:

Clinica Chimica Acta

Year:

1972

Language:

english

File:

PDF, 683 KB

english, 1972

22

Mitochondrial aspartate aminotransferase in myocardial infarction

Juhani Murros, Aarne Konttinen, Hannu Somer

Journal:

Clinica Chimica Acta

Year:

1973

Language:

english

File:

PDF, 160 KB

english, 1973

23

Reliability of serum LD isoenzyme determinations in the diagnosis of myocardial infarction

Aarne Konttinen, Samuli Auvinen, Hannu Somer

Journal:

Clinica Chimica Acta

Year:

1974

Language:

english

File:

PDF, 212 KB

english, 1974

24

Creatine kinase activity and its isoenzyme pattern in heart mitochondria

Hannu Somer, Anja Uotila, Aarne Konttinen, Nils-Erik Saris

Journal:

Clinica Chimica Acta

Year:

1974

Language:

english

File:

PDF, 624 KB

english, 1974

25

A new cause of increased serum aspartate aminotransferase activity

Aarne Konttinen, Juhani Murros, Kaarina Ojala, Mikko Salaspuro, Hannu Somer, Jorma Räsänen

Journal:

Clinica Chimica Acta

Year:

1978

Language:

english

File:

PDF, 208 KB

english, 1978

26

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

Helena Pihko, Marjatta Lappi, Christina Raitta, Kimmo Sainio, Leena Valanne, Hannu Somer, Pirkko Santavuori

Journal:

Brain and Development

Year:

1995

Language:

english

File:

PDF, 938 KB

english, 1995

27

Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3)

Henna Haravuori, H. Annika Siitonen, Ibrahim Mahjneh, Peter Hackman, Laura Lahti, Hannu Somer, Leena Peltonen, Marjo Kestilä, Bjarne Udd

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 95 KB

english, 2004

28

ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle’s disease

Mervi Löfberg, Harri Lindholm, Hannu Näveri, Anna Majander, Anu Suomalainen, Anders Paetau, Anssi Sovijärvi, Matti Härkönen, Hannu Somer

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 70 KB

english, 2001

29

Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations

Ibrahim Mahjneh, Giampiero Marconi, Kate Bushby, Louise V.B Anderson, Henna Tolvanen-Mahjneh, Hannu Somer

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 422 KB

english, 2001

30

Welander distal myopathy outside the Swedish population: phenotype and genotype

Désirée von Tell, Hannu Somer, Bjarne Udd, Lars Edström, Kristian Borg, Gabrielle Åhlberg

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 58 KB

english, 2002

31

Antimyosin scintigraphy compared with MRI in inflammatory myopathies

Mervi Löfberg, Kristian Liewendahl, Antti Lamminen, Hannu Somer

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 135 KB

english, 1997

32

Abnormal expression of β-dystroglycan in a patient with limb-girdle muscular dystrophy (LGMD)

Mari Auranen, Seppo Soinila, Hannu Somer

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 131 KB

english, 1997

33

Linkage in tibial muscular dystrophy (TMD) on chromosome 2q31–33

Henna Haravuori, Paivi Makela-Bengsl, Bjarne Udd, Leena Pulkkinen, Juhani Partanen, Hannu Somer, Leena Peltonen

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 132 KB

english, 1997

34

Immunohistochemistry and ultrastructure of rimmed vacuolar fibers in tibial muscular dystrophy

Bjarne Udd, Hannu Somer, Anders Pactau, Hannu Kalimo

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 134 KB

english, 1997

35

Tibial muscular dystrophy – from clinical description to linkage on chromosome 2q31

Bjarne Udd, Henna Haravuori, Hannu Kalimo, Juhani Partanen, Leena Pulkkinen, Anders Paetau, Leena Peltonen, Hannu Somer

Journal:

Neuromuscular Disorders

Year:

1998

Language:

english

File:

PDF, 934 KB

english, 1998

36

Assignment of the Tibial Muscular Dystrophy Locus to Chromosome 2q31

Henna Haravuori, Päivi Mäkelä-Bengs, Bjarne Udd, Juhani Partanen, Leena Pulkkinen, Hannu Somer, Leena Peltonen

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 1.45 MB

english, 1998

37

“Nothing dehydrogenase” reaction as an artefact in serum isoenzyme analyses

Journal:

Clinica Chimica Acta

Year:

1975

Language:

english

File:

PDF, 999 KB

english, 1975

38

Demonstration of serum creatine kinase isoenzymes by fluorescence technique

Hannu Somer, Aarne Konttinen

Journal:

Clinica Chimica Acta

Year:

1972

Language:

english

File:

PDF, 399 KB

english, 1972

39

Creatine kinase isoenzymes in neuromuscular diseases

Hannu Somer, Victor Dubowitz, Märta Donner

Journal:

Journal of the Neurological Sciences

Year:

1976

Language:

english

File:

PDF, 471 KB

english, 1976

40

Enzyme release from isolated erythrocytes and lymphocytes in Duchenne muscular dystrophy

Journal:

Journal of the Neurological Sciences

Year:

1980

Language:

english

File:

PDF, 427 KB

english, 1980

41

Cerebrospinal fluid lysozyme and β2-microglobulin in neurosarcoidosis

Virpi Oksanen, Carola Grönhagen-Riska, Sari Tikanoja, Hannu Somer, Frej Fyhrquist

Journal:

Journal of the Neurological Sciences

Year:

1986

Language:

english

File:

PDF, 444 KB

english, 1986

42

Myasthenia gravis associated with multiple sclerosis: Epidemiological survey and immunological findings

Hannu Somer, Kiti Müller, Esko Kinnunen

Journal:

Journal of the Neurological Sciences

Year:

1989

Language:

english

File:

PDF, 594 KB

english, 1989

43

Lymphocytic β-adrenergic receptors in X-linked muscular dystrophy

Tiina Mäki, Hannu Somer, Helena Pihko, Mikael Lindlöf, Kimmo Kontula, Matti Härkönen

Journal:

Journal of the Neurological Sciences

Year:

1989

Language:

english

File:

PDF, 608 KB

english, 1989

44

Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy

Bjarne Udd, Juhani Rapola, Pekka Nokelainen, Eri Arikawa, Hannu Somer

Journal:

Journal of the Neurological Sciences

Year:

1992

Language:

english

File:

PDF, 1.10 MB

english, 1992

45

Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis

Auli Verkkoniemi, Raija Ylikoski, Juha O Rinne, Mirja Somer, Aki Hietaharju, Timo Erkinjuntti, Matti Viitanen, Hannu Kalimo, Matti Haltia

Journal:

Journal of the Neurological Sciences

Year:

2004

Language:

english

File:

PDF, 241 KB

english, 2004

46

Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)

Melissa J Spencer, James G Tidball, Louise V.B Anderson, Kate M.D Bushby, John B Harris, M.Rita Passos-Bueno, Hannu Somer, Mariz Vainzof, Mayana Zatz

Journal:

Journal of the Neurological Sciences

Year:

1997

Language:

english

File:

PDF, 1.44 MB

english, 1997

47

Serum gelsolin and rhabdomyolysis

Mervi Löfberg, Tiina Paunio, Riitta Tähtelä, Sari Kiuru, Hannu Somer

Journal:

Journal of the Neurological Sciences

Year:

1998

Language:

english

File:

PDF, 238 KB

english, 1998

48

Molecular characterization of McArdle’s disease in two large Finnish families

Claudio Bruno, Mervi Löfberg, Lucia Tamburino, Heidi Jänkälä, George M Hadjigeorgiou, Antonio L Andreu, Sara Shanske, Hannu Somer, Salvatore DiMauro

Journal:

Journal of the Neurological Sciences

Year:

1999

Language:

english

File:

PDF, 477 KB

english, 1999

49

Muscle-eye-brain disease (MEB)

Santavuori, Pirkko, Somer, Hannu, Sainio, Kimmo, Rapola, Juhani, Kruus, Sirkka, Nikitin, Tuija, Ketonen, Leena, Leisti, Jaakko

Journal:

Brain and Development

Year:

1989

Language:

english

File:

PDF, 3.36 MB

english, 1989

50

Benign muscular dystrophy with autosomal dominant inheritance

Somer, Hannu, Laulumaa, Veikko, Paljärvi, Leo, Partanen, Juhani, Lamminen, Antti, Pihko, Helena, Sariola, Hannu, Haltia, Matti

Journal:

Neuromuscular Disorders

Year:

1991

Language:

english

File:

PDF, 768 KB

english, 1991