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A 10‐year experience of outcome in chemotherapy‐treated hereditary retinoblastoma

Acta ophthalmologica (Oxford, England), 2014-08, Vol.92 (5), p.404-411

2014

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Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53

Hereditary cancer in clinical practice, 2020-01, Vol.18 (1), p.1-1, Article 1

2020

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Brachytherapy in Multimodality Treatment for Pediatric Malignant Tumors-A Karolinska University Hospital Program

Brachytherapy, 2016-05, Vol.15, p.S65-S65

2016

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A comprehensive population-based study of malignant ovarian tumors, including histologic and immunohistochemical review, in children and adolescents 0–19 years old in Sweden between 1970 and 2014

Gynecologic oncology, 2024-05, Vol.184, p.206-213

2024

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Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer

Nature genetics, 2018-07, Vol.50 (7), p.944-950

2018

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Five-Year Follow-up After Multimodal Treatment Incorporating HDR Brachytherapy for Bladder Prostate Rhabdomyosarcoma in Children

International journal of radiation oncology, biology, physics, 2022-06, Vol.113 (2), p.355-359

2022

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A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Journal of medical genetics, 2022-02, Vol.59 (2), p.141

2022

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Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary TP53 -Related Cancer Syndrome Study (SWEP53)

Cancers, 2022-01, Vol.14 (2), p.380

2022

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Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience

Cancer, 2021-02, Vol.127 (4), p.628-638

2021

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Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

Pediatric blood & cancer, 2018-11, Vol.65 (11), p.e27301-n/a

2018

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Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer

Nature communications, 2015-01, Vol.6 (1), p.6125-6125, Article 6125

2015

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Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature

American journal of medical genetics. Part A, 2024-07, p.e63812

2024

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Intra‐arterial chemotherapy for retinoblastoma in Sweden – evaluation of treatment efficacy and complications

Acta ophthalmologica (Oxford, England), 2018-12, Vol.96 (8), p.e1040-e1041

2018

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Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study

The Lancet regional health. Europe, 2024, Vol.39, p.100881-100881, Article 100881

2024

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Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer

Genes chromosomes & cancer, 2014-07, Vol.53 (7), p.634-638

2014

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Birth characteristics and Wilms tumors in children in the Nordic countries: A register‐based case–control study

International journal of cancer, 2011-05, Vol.128 (9), p.2166-2173

2011

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Malignant ectomesenchymoma in children and adolescents: Report from the Cooperative Weichteilsarkom Studiengruppe (CWS)

Pediatric blood & cancer, 2013-02, Vol.60 (2), p.224-229

2013

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Incidence and survival analyses in children with solid tumours diagnosed in Sweden between 1983 and 2007

Acta Paediatrica, 2011-05, Vol.100 (5), p.750-757

2011

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Incidence and Survival Analyses in Children with Solid Tumours Diagnosed in Sweden 1983-2007

Acta paediatrica, 2011, Vol.100 (5), p.750

2011

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MALIGNANT ECTOMESENCHYMOMA TREATED IN THE COOPERATIVE WEICHTEILSARKOM STUDIENGRUPPE (CWS)

Pediatric blood & cancer, 2010, Vol.55 (5), p.900

2010

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INCIDENCE AND SURVIVAL ANALYSES IN CHILDREN WITH SOLID TUMOURS DIAGNOSED IN SWEDEN 1983-2007

PEDIATRIC BLOOD & CANCER, 2010, Vol.55 (5), p.935

2010

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Wilms tumor in children--considerably improved survival

Läkartidningen, 2006-05, Vol.103 (18), p.1440-1443

2006

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Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11

Oncogene, 1990-06, Vol.5 (6), p.901-907

1990

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Preferential loss of maternal alleles in sporadic Wilms' tumour

Oncogene, 1990-11, Vol.5 (11), p.1665-1668

1990

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Pharmacokinetics of acyclovir in immunocompromized children with leukopenia and mucositis after chemotherapy: Can intravenous acyclovir be substituted by oral valacyclovir?

Medical and pediatric oncology, 2002-04, Vol.38 (4), p.240-246

2002

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A 10‐year experience of outcome in chemotherapy‐treated hereditary retinoblastoma

Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53

Brachytherapy in Multimodality Treatment for Pediatric Malignant Tumors-A Karolinska University Hospital Program

A comprehensive population-based study of malignant ovarian tumors, including histologic and immunohistochemical review, in children and adolescents 0–19 years old in Sweden between 1970 and 2014

Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer

Five-Year Follow-up After Multimodal Treatment Incorporating HDR Brachytherapy for Bladder Prostate Rhabdomyosarcoma in Children

A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Whole-Body MRI Surveillance-Baseline Findings in the Swedish Multicentre Hereditary TP53 -Related Cancer Syndrome Study (SWEP53)

Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience

Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers

Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer

Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature

Intra‐arterial chemotherapy for retinoblastoma in Sweden – evaluation of treatment efficacy and complications

Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study

Confined trisomy 8 mosaicism of meiotic origin: A rare cause of aneuploidy in childhood cancer

Birth characteristics and Wilms tumors in children in the Nordic countries: A register‐based case–control study

Malignant ectomesenchymoma in children and adolescents: Report from the Cooperative Weichteilsarkom Studiengruppe (CWS)

Incidence and survival analyses in children with solid tumours diagnosed in Sweden between 1983 and 2007

Incidence and Survival Analyses in Children with Solid Tumours Diagnosed in Sweden 1983-2007

MALIGNANT ECTOMESENCHYMOMA TREATED IN THE COOPERATIVE WEICHTEILSARKOM STUDIENGRUPPE (CWS)

INCIDENCE AND SURVIVAL ANALYSES IN CHILDREN WITH SOLID TUMOURS DIAGNOSED IN SWEDEN 1983-2007

Wilms tumor in children--considerably improved survival

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11

Preferential loss of maternal alleles in sporadic Wilms' tumour

Pharmacokinetics of acyclovir in immunocompromized children with leukopenia and mucositis after chemotherapy: Can intravenous acyclovir be substituted by oral valacyclovir?

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