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Thiotepa and melphalan based single, tandem, and triple high dose therapy and autologous stem cell transplantation for high risk neuroblastoma

Pediatric blood & cancer, 2012-12, Vol.59 (7), p.1190-1197

2012

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Ultrahigh-risk group within the high-risk neuroblastoma category

Journal of pediatric hematology/oncology, 2013-08, Vol.35 (6), p.e254-e259

2013

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Segregation of a Missense Variant in Enteric Smooth Muscle Actin γ -2 With Autosomal Dominant Familial Visceral Myopathy

Gastroenterology (New York, N.Y. 1943), 2012-12, Vol.143 (6), p.1482-1491.e3

2012

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Clinical outcome and occurrence of uveitis in children with idiopathic tubulointerstitial nephritis

Pediatric nephrology (Berlin, West), 2011-02, Vol.26 (2), p.291-299

2011

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Expression profiles of matrix metalloproteinases and their inhibitors in colonic inflammation related to pediatric inflammatory bowel disease

Scandinavian journal of gastroenterology, 2010-08, Vol.45 (7-8), p.862-871

2010

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High frequency of tumours in Mulibrey nanism

The Journal of pathology, 2009-06, Vol.218 (2), p.163-171

2009

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Three-generation familial visceral myopathy with alpha-actin-positive inclusion bodies in intestinal smooth muscle

Journal of clinical gastroenterology, 2009-05, Vol.43 (5), p.437-443

2009

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Fecal calprotectin mirrors inflammation of the distal ileum and bowel function after restorative proctocolectomy for pediatric‐onset ulcerative colitis

Inflammatory bowel diseases, 2010-03, Vol.16 (3), p.482-486

2010

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Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1)

Transplantation, 2007-05, Vol.83 (10), p.1316-1323

2007

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Acquired myopathic intestinal pseudo-obstruction may be due to autoimmune enteric leiomyositis

Gastroenterology (New York, N.Y. 1943), 2002-04, Vol.122 (4), p.1133-1139

2002

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Symptomatic response to Helicobacter pylori eradication in children with recurrent abdominal pain: double blind randomized placebo-controlled trial

Journal of clinical gastroenterology, 2004-09, Vol.38 (8), p.646-650

2004

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Zygomycosis Presenting a Major Clinical Challenge: Case Report on Rhizomucor pusillus Infection in a Stem-Cell-Transplant Recipient

Mycopathologia (1975), 2011-09, Vol.172 (3), p.241-245

2011

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Cerebroretinal microangiopathy with calcifications and cysts: Characterization of the skeletal phenotype

American journal of medical genetics. Part A, 2011-06, Vol.155A (6), p.1322-1328

2011

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Acquired myopathic intestinal pseudo-obstruction may be due to autoimmune enteric leiomyositis

Gastroenterology (New York, N.Y. 1943), 2002-04, Vol.122 (4), p.1133-1139

2002

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Absence of human bocavirus from deceased fetuses and their mothers

Journal of clinical virology, 2010-02, Vol.47 (2), p.186-188

2010

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Metalloelastase (MMP-12) is upregulated in the gut of pediatric patients with potential celiac disease and in type 1 diabetes

Scandinavian journal of gastroenterology, 2005-12, Vol.40 (12), p.1413-1422

2005

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Gracile syndrome – BCS1L mutation as cause of complex III deficiency and iron overload

Mitochondrion, 2006-10, Vol.6 (5), p.26

2006

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Gonadoblastoma and Dysgerminoma Associated with XY Gonadal Dysgenesis in an Adolescent with Chronic Renal Failure: A Case of Frasier Syndrome

Journal of pediatric & adolescent gynecology, 2002-06, Vol.15 (3), p.145-149

2002

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Enhanced absorption of macromolecules : A secondary factor in Crohn's disease

Digestive diseases and sciences, 1996-07, Vol.41 (7), p.1423-1428

1996

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Gonadoblastoma and Dysgerminoma Associated with XY Gonadal Dysgenesis in an Adolescent with Chronic Renal Failure

Journal of pediatric & adolescent gynecology, 2002-06, Vol.15 (3), p.145-149

2002

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Importance of histopathological examination of the placenta

Duodecim (Helsinki, Finland : 1961), 2011, Vol.127 (5), p.464

Karikoski, Riitta

2011

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Abnormal embryogenesis in the etiology of ectopic pregnancy

Gynecologic and obstetric investigation, 1993-01, Vol.36 (3), p.158-162

1993

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The 48,XXYY syndrome: A case detected by maternal serum alpha-fetoprotein screening

Prenatal diagnosis, 1994-07, Vol.14 (7), p.644-645

1994

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Castleman's disease of the mesentery in a child: A case of seven years' duration without typical x-ray findings

Medical and pediatric oncology, 1997-05, Vol.28 (5), p.362-365

1997

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Thiotepa and melphalan based single, tandem, and triple high dose therapy and autologous stem cell transplantation for high risk neuroblastoma

Ultrahigh-risk group within the high-risk neuroblastoma category

Segregation of a Missense Variant in Enteric Smooth Muscle Actin γ -2 With Autosomal Dominant Familial Visceral Myopathy

Clinical outcome and occurrence of uveitis in children with idiopathic tubulointerstitial nephritis

Expression profiles of matrix metalloproteinases and their inhibitors in colonic inflammation related to pediatric inflammatory bowel disease

High frequency of tumours in Mulibrey nanism

Three-generation familial visceral myopathy with alpha-actin-positive inclusion bodies in intestinal smooth muscle

Fecal calprotectin mirrors inflammation of the distal ileum and bowel function after restorative proctocolectomy for pediatric‐onset ulcerative colitis

Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1)

Acquired myopathic intestinal pseudo-obstruction may be due to autoimmune enteric leiomyositis

Symptomatic response to Helicobacter pylori eradication in children with recurrent abdominal pain: double blind randomized placebo-controlled trial

Zygomycosis Presenting a Major Clinical Challenge: Case Report on Rhizomucor pusillus Infection in a Stem-Cell-Transplant Recipient

Cerebroretinal microangiopathy with calcifications and cysts: Characterization of the skeletal phenotype

Acquired myopathic intestinal pseudo-obstruction may be due to autoimmune enteric leiomyositis

Absence of human bocavirus from deceased fetuses and their mothers

Metalloelastase (MMP-12) is upregulated in the gut of pediatric patients with potential celiac disease and in type 1 diabetes

Gracile syndrome – BCS1L mutation as cause of complex III deficiency and iron overload

Gonadoblastoma and Dysgerminoma Associated with XY Gonadal Dysgenesis in an Adolescent with Chronic Renal Failure: A Case of Frasier Syndrome

Enhanced absorption of macromolecules : A secondary factor in Crohn's disease

Gonadoblastoma and Dysgerminoma Associated with XY Gonadal Dysgenesis in an Adolescent with Chronic Renal Failure

Importance of histopathological examination of the placenta

Abnormal embryogenesis in the etiology of ectopic pregnancy

The 48,XXYY syndrome: A case detected by maternal serum alpha-fetoprotein screening

Castleman's disease of the mesentery in a child: A case of seven years' duration without typical x-ray findings

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