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Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood

Clinical cancer research, 2017-06, Vol.23 (11), p.e32-e37

2017

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Constitutional mismatch repair-deficiency syndrome

Haematologica (Roma), 2010-05, Vol.95 (5), p.699-701

2010

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Transport spectroscopy of symmetry-broken insulating states in bilayer graphene

Nature nanotechnology, 2012-01, Vol.7 (3), p.156-160

2012

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Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)

Journal of Medical Genetics, 2014-06, Vol.51 (6), p.355-365

2014

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Cancer incidence and surveillance strategies in individuals with RASopathies

American journal of medical genetics. Part C, Seminars in medical genetics, 2022-12, Vol.190 (4), p.530-540

2022

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Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-05, Vol.157C (2), p.83-89

2011

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Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

Cancers, 2022-06, Vol.14 (13), p.3083

2022

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The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

Blood, 2005-09, Vol.106 (6), p.2183-2185

2005

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Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Clinical cancer research, 2017-07, Vol.23 (13), p.e123-e132

2017

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Predisposition to cancer in children and adolescents

The lancet child & adolescent health, 2021-02, Vol.5 (2), p.142-154

2021

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Retrieval of Cloud Properties Using CALIPSO Imaging Infrared Radiometer. Part I: Effective Emissivity and Optical Depth

Journal of applied meteorology and climatology, 2012-07, Vol.51 (7), p.1407-1425

2012

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Molecular complete remission following combination treatment of daratumumab and venetoclax in an adolescent with relapsed mixed phenotype acute leukemia

Annals of hematology, 2023-03, Vol.102 (3), p.669-672

2023

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Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome

Haematologica (Roma), 2024-02, Vol.109 (2), p.422-430

2024

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Health Behavior and Cancer Prevention among Adults with Li-Fraumeni Syndrome and Relatives in Germany-A Cohort Description

Current oncology (Toronto), 2022-10, Vol.29 (10), p.7768-7778

2022

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Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Journal of hematology and oncology, 2024-04, Vol.17 (1), p.26-26, Article 26

2024

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Radiative forcing by well-mixed greenhouse gases: Estimates from climate models in the Intergovernmental Panel on Climate Change (IPCC) Fourth Assessment Report (AR4)

Journal of Geophysical Research - Atmospheres, 2006-07, Vol.111 (D14), p.D14317-n/a

2006

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Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG)

Familial cancer, 2021-10, Vol.20 (4), p.317-325

2021

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TP53, ETV6 and RUNX1 germline variants in a case series of patients developing secondary neoplasms after treatment for childhood acute lymphoblastic leukemia

Haematologica (Roma), 2019-09, Vol.104 (9), p.e402-e405

2019

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Germline KRAS mutations cause Noonan syndrome

Nature genetics, 2006-03, Vol.38 (3), p.331-336

2006

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Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group

Journal of experimental & clinical cancer research, 2023-01, Vol.42 (1), p.21-21, Article 21

2023

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Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour

Journal of medical genetics, 2011-07, Vol.48 (7), p.473-476

2011

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Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood

Clinical cancer research, 2017-07, Vol.23 (13), p.e107-e114

2017

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An improved algorithm for retrieving surface downwelling longwave radiation from satellite measurements

Journal of Geophysical Research - Atmospheres, 2007-08, Vol.112 (D15), p.D15102-n/a

2007

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Breast cancer characteristics and surgery among women with Li‐Fraumeni syndrome in Germany—A retrospective cohort study

Cancer medicine (Malden, MA), 2021-11, Vol.10 (21), p.7747-7758

2021

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Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood

Constitutional mismatch repair-deficiency syndrome

Transport spectroscopy of symmetry-broken insulating states in bilayer graphene

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)

Cancer incidence and surveillance strategies in individuals with RASopathies

Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes

Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

Predisposition to cancer in children and adolescents

Retrieval of Cloud Properties Using CALIPSO Imaging Infrared Radiometer. Part I: Effective Emissivity and Optical Depth

Molecular complete remission following combination treatment of daratumumab and venetoclax in an adolescent with relapsed mixed phenotype acute leukemia

Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome

Health Behavior and Cancer Prevention among Adults with Li-Fraumeni Syndrome and Relatives in Germany-A Cohort Description

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Radiative forcing by well-mixed greenhouse gases: Estimates from climate models in the Intergovernmental Panel on Climate Change (IPCC) Fourth Assessment Report (AR4)

Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG)

TP53, ETV6 and RUNX1 germline variants in a case series of patients developing secondary neoplasms after treatment for childhood acute lymphoblastic leukemia

Germline KRAS mutations cause Noonan syndrome

Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group

Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour

Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood

An improved algorithm for retrieving surface downwelling longwave radiation from satellite measurements

Breast cancer characteristics and surgery among women with Li‐Fraumeni syndrome in Germany—A retrospective cohort study

Age-Dependent Presentation and Clinical Course of 1465 Patients Aged 0 to Less than 18 Years with Ovarian or Testicular Germ Cell Tumors; Data of the MAKEI 96 Protocol Revisited in the Light of Prenatal Germ Cell Biology

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