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An immunocapture-LC-MS-based assay for serum SPINK1 allows simultaneous quantification and detection of SPINK1 variants

Analytical and bioanalytical chemistry, 2018-02, Vol.410 (6), p.1679-1688

2018

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Heterogeneous SSTR2 target expression and a novel KIAA1549::BRAF fusion clone in a progressive metastatic lesion following 177Lutetium-DOTATATE molecular radiotherapy in neuroblastoma: a case report

Frontiers in oncology, 2024, Vol.14, p.1408729

2024

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Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma

Molecular cancer, 2024-08, Vol.23 (1), p.180-12, Article 180

2024

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Sustained Response to Entrectinib in an Infant With a Germline ALKAL2 Variant and Refractory Metastatic Neuroblastoma With Chromosomal 2p Gain and Anaplastic Lymphoma Kinase and Tropomyosin Receptor Kinase Activation

JCO precision oncology, 2022-01, Vol.6 (6), p.e2100271

2022

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The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden

Journal of translational medicine, 2023, Vol.21 (1), p.342-342, Article 342

2023

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MAPK inhibitors induce serine peptidase inhibitor Kazal type 1 (SPINK1) secretion in BRAF V600E‐mutant colorectal adenocarcinoma

Molecular oncology, 2018-02, Vol.12 (2), p.224-238

2018

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Pancreatectomies for pancreatic neoplasms in pediatric and adolescent age: A single institution experience

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2018-03, Vol.18 (2), p.204-207

2018

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Technique for strand-specific gene-expression analysis and monitoring of primer-independent cDNA synthesis in reverse transcription

BioTechniques, 2012-04, Vol.52 (4), p.263-270

2012

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Clinical response of the novel activating ALK-I1171T mutation in neuroblastoma to the ALK inhibitor ceritinib

Cold Spring Harbor molecular case studies, 2018-08, Vol.4 (4), p.a002550

2018

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A Phase II Trial of a Personalized, Dose-Intense Administration Schedule of 177Lutetium-DOTATATE in Children With Primary Refractory or Relapsed High-Risk Neuroblastoma–LuDO-N

Frontiers in pediatrics, 2022, Vol.10, p.836230

2022

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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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Influence of Surgical Excision on the Survival of Patients With Stage 4 High-Risk Neuroblastoma: A Report From the HR-NBL1/SIOPEN Study

Journal of clinical oncology, 2020-09, Vol.38 (25), p.2902-2915

2020

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Extendable blocking probe in reverse transcription for analysis of RNA variants with superior selectivity

Nucleic acids research, 2015-01, Vol.43 (1), p.e4-e4

2015

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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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Percutaneously inserted ventriculo-ureteral shunt as a salvage treatment in paediatric hydrocephalus: a technical note

Child's nervous system, 2023-01, Vol.39 (1), p.249-254

2023

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Evaluation of the expression levels of BRAFV600E mRNA in primary tumors of thyroid cancer using an ultrasensitive mutation assay

BMC cancer, 2020-05, Vol.20 (1), p.1-368, Article 368

2020

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Highly sensitive detection of EGFR L858R mutation at the mRNA level

Analytical biochemistry, 2022-10, Vol.654, p.114799-114799, Article 114799

2022

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Improved Local Control by Extensive Surgery in High-Risk Neuroblastoma May Be Dependent on Adjuvant Radiotherapy

Journal of clinical oncology, 2017-06, Vol.35 (17), p.1965-1966

2017

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Brachytherapy for rhabdomyosarcoma: Survey of international clinical practice and development of guidelines

Radiotherapy and oncology, 2024-06, Vol.195, p.110273, Article 110273

2024

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Tumor expression of human chorionic gonadotropin beta mRNA and prognosis of prostate cancer treated by radical prostatectomy

Scandinavian journal of clinical and laboratory investigation, 2019-08, Vol.79 (6), p.424-430

2019

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Abstract B060: Clonal composition of αβ and γδ T cells in primary human neuroblastoma tumors – Is every child unique?

Cancer research (Chicago, Ill.), 2024-09, Vol.84 (17_Supplement), p.B060-B060

2024

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Abstract 4727: Large scale drug response comparison across different neuroblastoma cell model systems

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.4727-4727

2024

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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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Relative levels of SCCA2 and SCCA1 mRNA in primary tumors predicts recurrent disease in squamous cell cancer of the head and neck

International journal of cancer, 2001-01, Vol.95 (1), p.39-43

2001

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An immunocapture-LC-MS-based assay for serum SPINK1 allows simultaneous quantification and detection of SPINK1 variants

Heterogeneous SSTR2 target expression and a novel KIAA1549::BRAF fusion clone in a progressive metastatic lesion following 177Lutetium-DOTATATE molecular radiotherapy in neuroblastoma: a case report

Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma

Sustained Response to Entrectinib in an Infant With a Germline ALKAL2 Variant and Refractory Metastatic Neuroblastoma With Chromosomal 2p Gain and Anaplastic Lymphoma Kinase and Tropomyosin Receptor Kinase Activation

The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden

MAPK inhibitors induce serine peptidase inhibitor Kazal type 1 (SPINK1) secretion in BRAF V600E‐mutant colorectal adenocarcinoma

Pancreatectomies for pancreatic neoplasms in pediatric and adolescent age: A single institution experience

Technique for strand-specific gene-expression analysis and monitoring of primer-independent cDNA synthesis in reverse transcription

Clinical response of the novel activating ALK-I1171T mutation in neuroblastoma to the ALK inhibitor ceritinib

A Phase II Trial of a Personalized, Dose-Intense Administration Schedule of 177Lutetium-DOTATATE in Children With Primary Refractory or Relapsed High-Risk Neuroblastoma–LuDO-N

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

Influence of Surgical Excision on the Survival of Patients With Stage 4 High-Risk Neuroblastoma: A Report From the HR-NBL1/SIOPEN Study

Extendable blocking probe in reverse transcription for analysis of RNA variants with superior selectivity

A Novel Standard for Systematic Reporting of Neuroblastoma Surgery: The International Neuroblastoma Surgical Report Form (INSRF): A Joint Initiative by the Pediatric Oncological Cooperative Groups SIOPEN∗, COG∗∗, and GPOH

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

Percutaneously inserted ventriculo-ureteral shunt as a salvage treatment in paediatric hydrocephalus: a technical note

Evaluation of the expression levels of BRAFV600E mRNA in primary tumors of thyroid cancer using an ultrasensitive mutation assay

Highly sensitive detection of EGFR L858R mutation at the mRNA level

Improved Local Control by Extensive Surgery in High-Risk Neuroblastoma May Be Dependent on Adjuvant Radiotherapy

Brachytherapy for rhabdomyosarcoma: Survey of international clinical practice and development of guidelines

Tumor expression of human chorionic gonadotropin beta mRNA and prognosis of prostate cancer treated by radical prostatectomy

Abstract B060: Clonal composition of αβ and γδ T cells in primary human neuroblastoma tumors – Is every child unique?

Abstract 4727: Large scale drug response comparison across different neuroblastoma cell model systems

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

Relative levels of SCCA2 and SCCA1 mRNA in primary tumors predicts recurrent disease in squamous cell cancer of the head and neck

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