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1

Syndrome X in testicularcancer survivors

Mervi Taskinen, Ulla Saarinen-Pihkala, Liisa Hovi, Marita Lipsanen-Nyman

Journal:

Year:

2001

Language:

english

File:

PDF, 57 KB

english, 2001

2

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, Jennifer Skaug, Kazuhiko Nakabayashi, Brenda Finucane, Danielle Hartung, Micheil Innes, Batsheva Kerem, Małgorzata J. Nowaczyk, Joseph Rivlin, Wendy Rob

Journal:

The American Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 208 KB

english, 2006

3

Novel mutations in the TRIM37 gene in Mulibrey Nanism

Riikka H. Hämäläinen, Kristiina Avela, Julie A. Lambert, Jukka Kallijärvi, Wafaa Eyaid, Jürgen Gronau, Andrew P. Ignaszewski, Deborah McFadden, Giovanni Sorge, Marita Lipsanen-Nyman, Anna-Elina Lehesj

Journal:

Year:

2004

Language:

english

File:

PDF, 495 KB

english, 2004

4

Cohen syndrome: evaluation of its cardiac, endocrine and radiological features

Satu Kivitie-Kallio, Marianne Eronen, Marita Lipsanen-Nyman, Eino Marttinen, Reijo Norio

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 474 KB

english, 1999

5

High frequency of tumours in Mulibrey nanism

Niklas Karlberg, Susann Karlberg, Riitta Karikoski, Sakari Mikkola, Marita Lipsanen-Nyman, Hannu Jalanko

Journal:

The Journal of Pathology

Year:

2009

Language:

english

File:

PDF, 636 KB

english, 2009

6

Assessment of mulibrey nanism cardiopathy with functional magnetic resonance imaging

S. Kokki, K. Lauerma, M. Kupari, M. Lipsanen-Nyman, P. Hekali

Journal:

Magnetic Resonance Materials in Physics, Biology and Medicine

Year:

2000

Language:

english

File:

PDF, 208 KB

english, 2000

7

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

M. Lehto, C. Wipemo, S.-A. Ivarsson, C. Lindgren, M. Lipsanen-Nyman, J. Weng, L. Wibell, E. Widén, T. Tuomi, L. Groop

Journal:

Year:

1999

Language:

english

File:

PDF, 108 KB

english, 1999

8

Cardiac Dysfunction in Children with Mulibrey Nanism

A. Eerola, J.I. Pihkala, N. Karlberg, M. Lipsanen-Nyman, E. Jokinen

Journal:

Pediatric Cardiology

Year:

2007

Language:

english

File:

PDF, 90 KB

english, 2007

9

Risk factors for reduced areal bone mineral density in young adults with stem cell transplantation in childhood

Mervi Taskinen, Kristiina Kananen, Matti Välimäki, Eliisa Löyttyniemi, Liisa Hovi, Ulla Saarinen-Pihkala, Marita Lipsanen-Nyman

Journal:

Pediatric Transplantation

Year:

2006

Language:

english

File:

PDF, 112 KB

english, 2006

10

10.1038/77053

Avela, Kristiina, Lipsanen-Nyman, Marita, Idänheimo, Niina, Seemanová, Eva, Rosengren, Sally, Mäkelä, Tomi P., Perheentupa, Jaakko, Chapelle, Albert de la, Lehesjoki, Anna-Elina

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 634 KB

english, 2000

11

Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas

Karlberg, Susann, Lipsanen-Nyman, Marita, Lassus, Heini, Kallijärvi, Jukka, Lehesjoki, Anna-Elina, Butzow, Ralf

Journal:

Modern Pathology

Year:

2009

Language:

english

File:

PDF, 432 KB

english, 2009

12

Mulibrey heart disease: clinical manifestations, long-term course, and results of pericardiectomy in a series of 49 patients born before 1985

M. Lipsanen-Nyman, J. Perheentupa, J. Rapola, A. Sovijärvi, M. Kupari

Journal:

ACC Current Journal Review

Year:

2003

Language:

english

File:

PDF, 36 KB

english, 2003

13

Growth hormone treatment of short children born small-for-gestational-age: the Nordic Multicentre Trial

M Boguszewski, K Albertsson-Wikland, S Aronsson, J Gustafsson, L Hagenas, U Westgren, O Westphal, M Lipsanen-Nyman, I Sipilä, P Gellert, J Müller, B Madsen

Journal:

Acta Paediatrica

Year:

1998

Language:

english

File:

PDF, 113 KB

english, 1998

14

Restriction Site-Specific Methylation Studies of Imprinted Genes with Quantitative Real-Time PCR

Bruce, S., Hannula-Jouppi, K., Lindgren, C. M., Lipsanen-Nyman, M., Kere, J.

Journal:

Clinical Chemistry

Year:

2008

Language:

english

File:

PDF, 264 KB

english, 2008

15

Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA

Katariina Hannula, Marita Lipsanen-Nyman, Stephen W. Scherer, Christer Holmberg, Pia Höglund, Juha Kere

Journal:

Year:

2001

Language:

english

File:

PDF, 283 KB

english, 2001

16

Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia

Maria Sandbacka, Sara Bruce, Mervi Halttunen, Minna Puhakka, Päivi Lahermo, Katariina Hannula-Jouppi, Marita Lipsanen-Nyman, Juha Kere, Kristiina Aittomäki, Hannele Laivuori

Journal:

Fertility and Sterility

Year:

2011

Language:

english

File:

PDF, 91 KB

english, 2011

17

Impaired glucose tolerance and dyslipidaemia as late effects after bone-marrow transplantation in childhood

Menrvi Taskinen, Ulla M Saarinen-Pihkala, Liisa Hovi, Mania Lipsanen-Nyman

Journal:

Year:

2000

Language:

english

File:

PDF, 88 KB

english, 2000

18

A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region

Katariina Hannula, Marita Lipsanen-Nyman, Tero Kontiokari, Juha Kere

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 1.30 MB

english, 2001

19

The TRIM37 Gene Encodes a Peroxisomal RING-B-Box-Coiled-Coil Protein: Classification of Mulibrey Nanism as a New Peroxisomal Disorder

Jukka Kallijärvi, Kristiina Avela, Marita Lipsanen-Nyman, Ismo Ulmanen, Anna-Elina Lehesjoki

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 909 KB

english, 2002

20

TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase

Jukka Kallijärvi, Ulla Lahtinen, Riikka Hämäläinen, Marita Lipsanen-Nyman, Jorma J. Palvimo, Anna-Elina Lehesjoki

Journal:

Experimental Cell Research

Year:

2005

Language:

english

File:

PDF, 414 KB

english, 2005

21

Growth and Growth Hormone Therapy in Subjects With Mulibrey Nanism

Karlberg, N., Jalanko, H., Lipsanen-Nyman, M.

Journal:

Year:

2007

Language:

english

File:

PDF, 615 KB

english, 2007

22

Suppressed Bone Turnover in Obesity: A Link to Energy Metabolism? A Case-Control Study

Viljakainen, Heli, Ivaska, Kaisa K., Paldánius, Päivi, Lipsanen-Nyman, Marita, Saukkonen, Tero, Pietiläinen, Kirsi H., Andersson, Sture, Laitinen, Kalevi, Mäkitie, Outi

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2014

Language:

english

File:

PDF, 167 KB

english, 2014

23

Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7

Hannula-Jouppi, Katariina, Muurinen, Mari, Lipsanen-Nyman, Marita, Reinius, Lovisa E, Ezer, Sini, Greco, Dario, Kere, Juha

Journal:

Year:

2014

Language:

english

File:

PDF, 1.06 MB

english, 2014

24

Association of intramyocellular, intraperitoneal and liver fat with glucose tolerance in severely obese adolescents

Saukkonen, T., Heikkinen, S., Hakkarainen, A., Hakkinen, A.-M., van Leemput, K., Lipsanen-Nyman, M., Lundbom, N.

Journal:

European Journal of Endocrinology

Year:

2010

Language:

english

File:

PDF, 153 KB

english, 2010

25

A Two-Base Deletion –439delGC in the Melanocortin-4 Receptor Promoter Associated with Early-Onset Obesity

Valli-Jaakola, Kaisa, Palvimo, Jorma J., Lipsanen-Nyman, Marita, Salomaa, Veikko, Peltonen, Leena, Kontula, Kimmo, Schalin-J&auml, ntti, Camilla

Journal:

Hormone Research

Year:

2006

Language:

english

File:

PDF, 180 KB

english, 2006

26

Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Prenatal and Postnatal Growth Retardation of Unknown Cause

Hannula, K., Lipsanen-Nyman, M., Kristo, P., Kaitila, I., Simola, K. O. J., Lenko, H. L., Tapanainen, P., Holmberg, C., Kere, J.

Journal:

Year:

2002

Language:

english

File:

PDF, 329 KB

english, 2002

27

Mulibrey Heart Disease: Clinical Manifestations, Long-Term Course, and Results of Pericardiectomy in a Series of 49 Patients Born Before 1985

Lipsanen-Nyman, M.

Journal:

Year:

2003

Language:

english

File:

PDF, 348 KB

english, 2003

28

Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients

Bruce, S., Hannula-Jouppi, K., Puoskari, M., Fransson, I., Simola, K. O. J., Lipsanen-Nyman, M., Kere, J.

Journal:

Journal of Medical Genetics

Year:

2010

Language:

english

File:

PDF, 281 KB

english, 2010

29

Insulin Resistance Syndrome in Subjects With Mutated RING Finger Protein TRIM37

Karlberg, N., Jalanko, H., Kallijarvi, J., Lehesjoki, A.-E., Lipsanen-Nyman, M.

Journal:

Year:

2005

Language:

english

File:

PDF, 132 KB

english, 2005

30

Identification and Characterization of Melanocortin-4 Receptor Gene Mutations in Morbidly Obese Finnish Children and Adults

Valli-Jaakola, Kaisa, Lipsanen-Nyman, Marita, Oksanen, Laura, Hollenberg, Anthony N., Kontula, Kimmo, Bjørbæk, Christian, Schalin-Jäntti, Camilla

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 281 KB

english, 2004

31

Failure of Sexual Maturation in Mulibrey Nanism

Karlberg, Susann, Tiitinen, Aila, Lipsanen-Nyman, Marita

Journal:

Boston Medical and Surgical Journal

Year:

2004

Language:

english

File:

PDF, 80 KB

english, 2004

32

Bone Characteristics and Their Determinants in Adolescents and Young Adults with Early-Onset Severe Obesity

Viljakainen, H. T., Valta, H., Lipsanen-Nyman, M., Saukkonen, T., Kajantie, E., Andersson, S., Mäkitie, O.

Journal:

Calcified Tissue International

Year:

2015

Language:

english

File:

PDF, 502 KB

english, 2015

33

Testicular Failure and Male Infertility in the Monogenic Mulibrey Nanism Disorder

Karlberg, Susann, Toppari, Jorma, Karlberg, Niklas, Nurmio, Mirja, Karikoski, Riitta, Jalanko, Hannu, Lipsanen-Nyman, Marita

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2011

Language:

english

File:

PDF, 2.34 MB

english, 2011

34

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of H19 Hypomethylation Associates with Phenotype Severity and Genital and Skeletal Anomalies

Bruce, Sara, Hannula-Jouppi, Katariina, Peltonen, Jari, Kere, Juha, Lipsanen-Nyman, Marita

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 234 KB

english, 2009

35

Insufficient Growth Hormone Secretion is Associated With Metabolic Syndrome After Allogeneic Stem Cell Transplantation in Childhood

Taskinen, Mervi, Lipsanen-Nyman, Marita, Tiitinen, Aila, Hovi, Liisa, Saarinen-Pihkala, Ulla M.

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2007

Language:

english

File:

PDF, 144 KB

english, 2007

36

Renal findings in patients with Mulibrey nanism

Sivunen, Johanna, Karlberg, Susann, Lohi, Jouko, Karlberg, Niklas, Lipsanen-Nyman, Marita, Jalanko, Hannu

Journal:

Pediatric Nephrology

Year:

2017

Language:

english

File:

PDF, 728 KB

english, 2017

37

Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children

Muurinen, Mari, Hannula-Jouppi, Katariina, Reinius, Lovisa E., Söderhäll, Cilla, Merid, Simon Kebede, Bergström, Anna, Melén, Erik, Pershagen, Göran, Lipsanen-Nyman, Marita, Greco, Dario, Kere, Juha

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 2.01 MB

english, 2017

38

Premature ovarian insufficiency and early depletion of the ovarian reserve in the monogenic Mulibrey nanism disorder

Karlberg, Susann, Tiitinen, Aila, Alfthan, Henrik, Lipsanen-Nyman, Marita

Journal:

Human Reproduction

Year:

2018

Language:

english

File:

PDF, 384 KB

english, 2018

39

Testicular Function and Bone in Young Men with Severe Childhood-Onset Obesity

Laakso, Saila, Viljakainen, Heli, Lipsanen-Nyman, Marita, Turpeinen, Ursula, Ivaska, Kaisa K., Anand-Ivell, Ravinder, Ivell, Richard, Mäkitie, Outi

Journal:

Hormone Research in Paediatrics

Year:

2018

Language:

english

File:

PDF, 218 KB

english, 2018

40

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of H19 Hypomethylation Associates with SRS Phenotype Severity and Genital and Skeletal Anomalies

Bruce, Sara, Hannula-Jouppi, Katariina, Peltonen, Jari, Kere, Juha, Lipsanen-Nyman, Marita

Journal:

Molecular Endocrinology

Year:

2009

File:

PDF, 70 KB

2009

41

Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity

Loid, Petra, Mustila, Taina, MÃ¤kitie, Riikka E., Viljakainen, Heli, KÃ¤mpe, Anders, Tossavainen, PÃ¤ivi, Lipsanen-Nyman, Marita, Pekkinen, Minna, MÃ¤kitie, Outi

Journal:

Frontiers in Endocrinology

Year:

2020

File:

PDF, 544 KB

2020