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Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study

Neurology, 2022-01, Vol.98 (1), p.e51

2022

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Total en bloc spondylectomy of T11 and spine shortening performed on a 17-month-old patient: art of the possible

European spine journal, 2020-12, Vol.29 (Suppl 2), p.145-148

2020

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Two Broad Categories Overlapping With Rheumatoid Arthritis Observed in Synovial Biopsies from Patients With Juvenile Idiopathic Arthritis

Arthritis & rheumatology (Hoboken, N.J.), 2024-07

2024

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Atrial fibrillation in a pediatric patient caused by an unusual malignant etiology: A case report

Frontiers in pediatrics, 2023-02, Vol.11, p.1051041

2023

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Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

Rheumatic & musculoskeletal diseases open, 2021-06, Vol.7 (2), p.e001646

2021

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Successful treatment of refractory mevalonate kinase deficiency with combination therapy targeting TNFα and IL1β

Rheumatology (Oxford, England), 2024-03

2024

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Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infection

The Journal of experimental medicine, 2020-11, Vol.217 (11)

2020

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Safety of reducing antibiotic use in children with febrile neutropenia: A systematic review

Pediatric hematology and oncology, 2022-10, Vol.39 (8), p.707-723

2022

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Atypical phenotype? The answer’s in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency

Rheumatology (Oxford, England), 2021-07, Vol.60 (7), p.e240-e242

2021

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Successful use of empagliflozin to treat neutropenia in two G6PC3‐deficient children: Impact of a mutation in SGLT5

Journal of inherited metabolic disease, 2022-07, Vol.45 (4), p.759-768

2022

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Clinical Spectrum of Ras-Associated Autoimmune Leukoproliferative Disorder (RALD)

Journal of clinical immunology, 2021, Vol.41 (1), p.51-58

2021

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Characterization and risk factors of hyperglycaemia during treatment of childhood hematologic malignancies

Diabetic medicine, 2022-02, Vol.39 (2), p.e14720-n/a

2022

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Rhabdomyosarcoma associated with germline TP53 alteration in children and adolescents: The French experience

Pediatric blood & cancer, 2020-09, Vol.67 (9), p.e28486-n/a

2020

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B-acute Lymphoblastic Leukemia With Hypereosinophilia Associated With Severe Cardiac Complications: A Clinical Case

Journal of pediatric hematology/oncology, 2021-01, Vol.43 (1), p.e51

2021

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High‐dose chemotherapy followed by autologous stem cell rescue in Wilms tumors: French report on toxicity and efficacy

Pediatric blood & cancer, 2022-03, Vol.69 (3), p.e29431-n/a

2022

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Environmental exposures related to parental habits in the perinatal period and the risk of Wilms' tumor in children

Cancer epidemiology, 2020-06, Vol.66, p.101706-101706, Article 101706

2020

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Detection of alternative lengthening of telomeres mechanism on tumor sections

Molecular biomedicine, 2021-10, Vol.2 (1), p.32-32, Article 32

2021

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Liver metastasis at diagnosis in children with nephroblastoma enrolled in SIOP2001 protocol: A French multicentric study

Pediatric blood & cancer, 2020-06, Vol.67 (6), p.e28201-n/a

2020

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Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome‐like phenotype and hypogammaglobulinemia

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1813-1820

2017

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DNAJB1‐PRKACA–positive metastatic fibrolamellar carcinoma with unknown primary in a pediatric patient

Pediatric blood & cancer, 2020-02, Vol.67 (2), p.e28060-n/a

2020

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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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94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation

Clinical immunology (Orlando, Fla.), 2024-05, Vol.262, p.110036, Article 110036

2024

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Transcriptomic profiling and immuno-histological characterization of synovial biopsies in juvenile idiopathic arthritis (JIA) suggest two broad categories, with significant overlap with rheumatoid arthritis (RA)

Arthritis & rheumatology (Hoboken, N.J.), 2024-05

2024

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Another elephant in the room : les soignants de pédiatrie et l’alimentation/hydratation en fin de vie

Médecine palliative, 2021-02, Vol.20 (1), p.32-40

2021

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Atrial fibrillation in a pediatric patient caused by an unusual malignant etiology: A case report

Frontiers in pediatrics, 2023, Vol.11, p.1051041-1051041

2023

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Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study

Total en bloc spondylectomy of T11 and spine shortening performed on a 17-month-old patient: art of the possible

Two Broad Categories Overlapping With Rheumatoid Arthritis Observed in Synovial Biopsies from Patients With Juvenile Idiopathic Arthritis

Atrial fibrillation in a pediatric patient caused by an unusual malignant etiology: A case report

Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

Successful treatment of refractory mevalonate kinase deficiency with combination therapy targeting TNFα and IL1β

Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infection

Safety of reducing antibiotic use in children with febrile neutropenia: A systematic review

Atypical phenotype? The answer’s in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency

Successful use of empagliflozin to treat neutropenia in two G6PC3‐deficient children: Impact of a mutation in SGLT5

Clinical Spectrum of Ras-Associated Autoimmune Leukoproliferative Disorder (RALD)

Characterization and risk factors of hyperglycaemia during treatment of childhood hematologic malignancies

Rhabdomyosarcoma associated with germline TP53 alteration in children and adolescents: The French experience

B-acute Lymphoblastic Leukemia With Hypereosinophilia Associated With Severe Cardiac Complications: A Clinical Case

High‐dose chemotherapy followed by autologous stem cell rescue in Wilms tumors: French report on toxicity and efficacy

Environmental exposures related to parental habits in the perinatal period and the risk of Wilms' tumor in children

Detection of alternative lengthening of telomeres mechanism on tumor sections

Liver metastasis at diagnosis in children with nephroblastoma enrolled in SIOP2001 protocol: A French multicentric study

Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome‐like phenotype and hypogammaglobulinemia

DNAJB1‐PRKACA–positive metastatic fibrolamellar carcinoma with unknown primary in a pediatric patient

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

94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation

Transcriptomic profiling and immuno-histological characterization of synovial biopsies in juvenile idiopathic arthritis (JIA) suggest two broad categories, with significant overlap with rheumatoid arthritis (RA)

Another elephant in the room : les soignants de pédiatrie et l’alimentation/hydratation en fin de vie

Atrial fibrillation in a pediatric patient caused by an unusual malignant etiology: A case report

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