S. Helena Pihko: search on Z-Library

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1

Pathology of Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Caused by the G1528C Mutation

Tyni, Tiina, Rapola, Juhani, Paetau, Anders, Palotie, Aarno, Pihko, Helena

Journal:

Fetal and Pediatric Pathology

Year:

1997

Language:

english

File:

PDF, 5.20 MB

english, 1997

2

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

3

Studies of carcino-fetal proteins. II. Biochemical comparison of α-fetoprotein from human fetuses and patients with hepatocellular cancer

Erkki Ruoslahti, Markku Seppälä, Helena Pihko, Pekka Vuopio

Journal:

International Journal of Cancer

Year:

1971

Language:

english

File:

PDF, 456 KB

english, 1971

4

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

5

Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA)

Dr. Tuula Koskinen, Dr. Kimmo Sainio, Dr. Juhani Rapola, Dr. Helena Pihko, Dr. Anders Paetau

Journal:

Year:

1994

Language:

english

File:

PDF, 668 KB

english, 1994

6

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

Tiina Tyni, Juhani Rapola, Aarno Palotie, Helena Pihko

Journal:

The Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 275 KB

english, 1997

7

A Juvenile Case of MELAS with T3271C Mitochondrial DNA Mutation

Stenqvist, Laura, Paetau, Anders, Valanne, Leena, Suomalainen, Anu, Pihko, Helena

Journal:

Pediatric Research

Year:

2005

Language:

english

File:

PDF, 581 KB

english, 2005

8

Ototoxicity in children with malignant brain tumors treated with the “8 in 1” chemotherapy protocol

Ilveskoski, Ismo, Saarinen, Ulla M., Wiklund, Tom, Perkkiö, Mikko, Salmi, Toivo T., Lanning, Marjatta, Mäkipernaa, Anne, Pihko, Helena

Journal:

Medical and Pediatric Oncology

Year:

1996

Language:

english

File:

PDF, 481 KB

english, 1996

9

Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies

Kaisa Silander, Päivi Meretoja, Vesa Juvonen, Jaakko Ignatius, Helena Pihko, Ari Saarinen, Tiina Wallden, Eila Herrgård, Pertti Aula, Marja-Liisa Savontaus

Journal:

Year:

1998

Language:

english

File:

PDF, 304 KB

english, 1998

10

Carcinoembryonic antigen and alpha fetoprotein in malignant tumors of the female genital tract

Markku Seppälä, Helena Pihko, Erkki Ruoslahti

Journal:

Year:

1975

Language:

english

File:

PDF, 385 KB

english, 1975

11

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

12

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

Anna Majander, Dr. Helena Pihko, Pirkko Santavuori

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 290 KB

english, 1995

13

18q deletions: Clinical, molecular, and brain MRI findings of 14 individuals

Tarja Linnankivi, Pentti Tienari, Mirja Somer, Marketta Kähkönen, Tuula Lönnqvist, Leena Valanne, Helena Pihko

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 234 KB

english, 2006

14

Cerebral palsy is characterized by protein mediators in cord serum

Tuula Kaukola, Ebenezer Satyaraj, Dhavalkumar D. Patel, Velizar T. Tchernev, Brian G. Grimwade, Stephen F. Kingsmore, Pentti Koskela, Outi Tammela, Leena Vainionpää, Helena Pihko, Tuula Äärimaa, Mikko

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 113 KB

english, 2004

15

Metabolic characterization of childhood brain tumors : Comparison of 18F-fluorodeoxyglucose and 11C-methionine positron emission tomography

Meri Utriainen, Liisa Metsähonkala, Toivo T. Salmi, Tapio Utriainen, Hannu Kalimo, Helena Pihko, Anne Mäkipernaa, Arja Harila-Saari, Sirkku Jyrkkiö, Jukka Laine, Kjell Någren, Heikki Minn

Journal:

Year:

2002

Language:

english

File:

PDF, 747 KB

english, 2002

16

Rabbit alpha-fetoprotein: normal levels and breakage tolerance with haptenated homologous alpha-fetoprotein

E. Ruoslahti, Helena Pihko, M. Becker, O. Mäkelä

Journal:

European Journal of Immunology

Year:

1975

Language:

english

File:

PDF, 411 KB

english, 1975

17

High level of alpha-fetoprotein in sera of adult mice

Helena Pihko, Erkki Ruoslahti

Journal:

International Journal of Cancer

Year:

1973

Language:

english

File:

PDF, 418 KB

english, 1973

18

18q− Syndrome: Brain MRI shows poor differentiation of gray and white matter on T2-weighted images

Tarja T. Linnankivi, Taina H. Autti, S. Helena Pihko, Mirja S. Somer, Pentti J. Tienari, Kari O. Wirtavuori, Leena K. Valanne

Journal:

Journal of Magnetic Resonance Imaging

Year:

2003

Language:

english

File:

PDF, 436 KB

english, 2003

19

Neurodevelopmental outcome in high-risk patients after renal transplantation in early childhood

Erik Qvist, Helena Pihko, Pia Fagerudd, Leena Valanne, Sirkka Lamminranta, Jukka Karikoski, Kimmo Sainio, Kai Rönnholm, Hannu Jalanko, Christer Holmberg

Journal:

Pediatric Transplantation

Year:

2002

Language:

english

File:

PDF, 104 KB

english, 2002

20

Neuroradiologic findings in children with renal transplantation under 5 years of age

Leena Valanne, Erik Qvist, Hannu Jalanko, Christer Holmberg, Helena Pihko

Journal:

Pediatric Transplantation

Year:

2004

Language:

english

File:

PDF, 265 KB

english, 2004

21

High-dose thiotepa with autologous bone marrow rescue in recurrent malignant oligodendroglioma: A case report

Ulla M. Saarinen, Helena Pihko, Anne Mäkipernaa

Journal:

Journal of Neuro-Oncology

Year:

1990

Language:

english

File:

PDF, 398 KB

english, 1990

22

Partial 11q trisomy syndrome

Helena Pihko, Eeva Therman, Irene A. Uchida

Journal:

Year:

1981

Language:

english

File:

PDF, 658 KB

english, 1981

23

Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance

K. Silander, Päivi Meretoja, Helena Pihko, Vesa Juvonen, Jouni Issakainen, Pertti Aula, Marja-Liisa Savontaus

Journal:

Year:

1997

Language:

english

File:

PDF, 71 KB

english, 1997

24

Screening ofBCS1Lmutations in severe neonatal disorders suspicious for mitochondrial cause

Vineta Fellman, Susanna Lemmelä, Antti Sajantila, Helena Pihko, Irma Järvelä

Journal:

Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 200 KB

english, 2008

25

Headache in children and adolescents after organ transplantation

Aki Uutela, Erik Qvist, Christer Holmberg, Helena Pihko, Hannu Jalanko

Journal:

Pediatric Transplantation

Year:

2009

Language:

english

File:

PDF, 140 KB

english, 2009

26

Low bone mass in patients with motor disability: prevalence and risk factors in 59 Finnish children

PÄIVI KILPINEN-LOISA, TAAVA PAASIO, MARTTI SOIVA, ULLA MAIJA RITANEN, PENTTI LAUTALA, PETRI PALMU, HELENA PIHKO, OUTI MÄKITIE

Journal:

Developmental Medicine & Child Neurology

Year:

2010

Language:

english

File:

PDF, 172 KB

english, 2010

27

Alpha-fetoprotein: Immunochemical Purification and Chemical Properties. Expression in Normal State and in Malignant and non-Malignant Liver Disease

Erkki Ruoslahti, Helena Pihko, Markku Seppälä

Journal:

Immunological Reviews

Year:

1974

Language:

english

File:

PDF, 6.91 MB

english, 1974

28

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

Pirkko Santavuori, Leena Valanne, Taina Autti, Matti Haltia, Helena Pihko, Kimmo Sainio

Journal:

European Journal of Paediatric Neurology

Year:

1998

Language:

english

File:

PDF, 635 KB

english, 1998

29

Mutations in CTC1, Encoding the CTS Telomere Maintenance Complex Component 1, Cause Cerebroretinal Microangiopathy with Calcifications and Cysts

Anne Polvi, Tarja Linnankivi, Tero Kivelä, Riitta Herva, James P. Keating, Outi Mäkitie, Davide Pareyson, Leena Vainionpää, Jenni Lahtinen, Iiris Hovatta, Helena Pihko, Anna-Elina Lehesjoki

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 922 KB

english, 2012

30

Pirkko Santavuori 1933–2004

Journal:

European Journal of Paediatric Neurology

Year:

2004

Language:

english

File:

PDF, 69 KB

english, 2004

31

Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations

Ulrike Schara, Hans-Jürgen Christen, Hacer Durmus, Marja Hietala, Kerstin Krabetz, Carmelo Rodolico, Gudrun Schreiber, Haluk Topaloglu, Beril Talim, Wolfgang Voss, Helena Pihko, Angela Abicht, Juliane

Journal:

European Journal of Paediatric Neurology

Year:

2010

Language:

english

File:

PDF, 521 KB

english, 2010

32

Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Tiina Tyni, Eeva Ekholm, Helena Pihko

Journal:

American Journal of Obstetrics and Gynecology

Year:

1998

Language:

english

File:

PDF, 30 KB

english, 1998

33

FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study

Anu Suomalainen, Jenni M Elo, Kirsi H Pietiläinen, Anna H Hakonen, Ksenia Sevastianova, Mari Korpela, Pirjo Isohanni, Sanna K Marjavaara, Tiina Tyni, Sari Kiuru-Enari, Helena Pihko, Niklas Darin, Katr

Journal:

The Lancet Neurology

Year:

2011

Language:

english

File:

PDF, 298 KB

english, 2011

34

EFFECT OF CHEMICAL MODIFICATION ON THE IMMUNO-GENICITY OF HOMOLOGOUS α-FETOPROTEIN

Erkki Ruoslahti, Helena Pihko

Journal:

Annals of the New York Academy of Sciences

Year:

1975

Language:

english

File:

PDF, 693 KB

english, 1975

35

Clinical features in a de novo interstitial deletion 15q13 to q15

Seppo Autio, Helena Pihko, Carola Tengström

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 449 KB

english, 1988

36

Bilateral alterations in somatosensory cortical processing in hemiplegic cerebral palsy

PÄIVI NEVALAINEN, ELINA PIHKO, HELENA MÄENPÄÄ, LEENA VALANNE, LAURI NUMMENMAA, LEENA LAURONEN

Journal:

Developmental Medicine & Child Neurology

Year:

2012

Language:

english

File:

PDF, 337 KB

english, 2012

37

The single chain nature of human group specific (Gc) protein

P. Kuusela, Helena Pihko

Journal:

Biochimica et Biophysica Acta (BBA) - Protein Structure

Year:

1972

Language:

english

File:

PDF, 199 KB

english, 1972

38

Clinical significance of urinary and serum hydroxyproline determination in sarcoidosis

Jouni Uitto, Paavo Tani, Helena Pihko

Journal:

Clinica Chimica Acta

Year:

1971

Language:

english

File:

PDF, 386 KB

english, 1971

39

Rabbit α-fetoprotein: Immunochemical purification and partial characterization

Helena Pihko, Jan Lindgren, Erkki Ruoslahti

Journal:

Immunochemistry

Year:

1973

Language:

english

File:

PDF, 1.44 MB

english, 1973

40

Carcinoembryonic antigen-like substance in gastric juice

Matti Vuento, Erkki Ruoslahti, Helena Pihko, Torgny Svenberg, Timo Ihamäki, Max Siurala

Journal:

Immunochemistry

Year:

1976

Language:

english

File:

PDF, 297 KB

english, 1976

41

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

42

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

Susanna Ranta, Helena Pihko, Pirkko Santavuori, Esa Tahvanainen, Albert de la Chapelle

Journal:

Neuromuscular Disorders

Year:

1995

Language:

english

File:

PDF, 342 KB

english, 1995

43

Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation

Tiina Tyni, Anna Majander, Hannu Kalimo, Juhani Rapola, Helena Pihko

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 911 KB

english, 1996

44

Pirkko Santavuori 1933–2004

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 53 KB

english, 2004

45

Skeletal dysplasia presenting as a neuromuscular disorder – report of three children

Jonas Bondestam, Helena Pihko, Sanna-Leena Vanhanen, Antti Brander, Sanna Toiviainen-Salo, Eino Marttinen, Outi Mäkitie

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 366 KB

english, 2007

46

Transient ischemic cerebral lesions during induction chemotherapy for acute lymphoblastic leukemia

Helena Pihko, Tiina Tyni, Kristina Virkola, Leena Valanne, Kimmo Sainio, Liisa Hovi, Ulla M. Saarinen

Journal:

The Journal of Pediatrics

Year:

1993

Language:

english

File:

PDF, 2.03 MB

english, 1993

47

Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients

Tiina Tyni, Aarno Palotie, Lasse Viinikka, Leena Valanne, Matti K. Salo, Ulrika von Döbeln, Sandra Jackson, Ronald Wanders, Nikolaos Venizelos, Helena Pihko

Journal:

The Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 919 KB

english, 1997

48

Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria

Vineta Fellman, Juhani Rapola, Helena Pihko, Teppo Varilo, Kari O Raivio

Journal:

Year:

1998

Language:

english

File:

PDF, 75 KB

english, 1998

49

Ophthalmologic findings in long-chain 3-hydroxyacyl-Coa dehydrogenase deficiency caused by the G1528C mutation: A new type of hereditary metabolic chorioretinopathy

Tiina Tyni, Tero Kivelä, Marjatta Lappi, Paula Summanen, Eeva Nikoskelainen, Helena Pihko

Journal:

Year:

1998

Language:

english

File:

PDF, 8.49 MB

english, 1998

50

Hypertensive encephalopathy in children with malignant disease

Journal:

Pediatric Neurology

Year:

1997

Language:

english

File:

PDF, 64 KB

english, 1997