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485 results on '"PELLIER, ISABELLE"'

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51. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

52. The Impact of Donor Type on Long-Term Health Status and Quality of Life after Allogeneic Hematopoietic Stem Cell Transplantation for Childhood Acute Leukemia: A Leucémie de l'Enfant et de L'Adolescent Study

55. Educational outcomes in siblings of childhood leukemia survivors: Factors associated with school difficulties and comparison with general population.

56. Impact of childhood leukemia on siblings: their long-term perception of family functioning and its relationship with their psychosocial characteristics using structural equation modeling

57. Impact of age at diagnosis, sex, and immunopathological manifestations in 886 patients with pediatric chronic immune thrombocytopenia

58. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

59. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

60. Molecular and clinicopathologic characterization of pediatric histiocytoses

61. Symptomatic osteonecrosis in French survivors of childhood and adolescent leukemia: a clinical and MRI study of LEA cohort

62. Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure

64. Prevention of Infections During Primary Immunodeficiency

65. Invasive Pneumococcal Disease in Children Can Reveal a Primary Immunodeficiency

66. Cardiac and Vascular Risks Are the Essential Parameters for Long-Term Surveillance of Lower Risk Childhood Acute Leukemia Survivors

68. Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

69. Brothers and sisters of childhood acute leukemia survivors: Their long‐term quality of life and its determinants

71. Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

72. Maternal residential pesticide use during pregnancy and risk of malignant childhood brain tumors: A pooled analysis of the ESCALE and ESTELLE studies (SFCE)

74. Molecular and clinicopathologic characterization of pediatric histiocytoses.

75. Extended Spectrum of Human Glucose-6-Phosphatase Catalytic Subunit 3 Deficiency: Novel Genotypes and Phenotypic Variability in Severe Congenital Neutropenia

76. Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia

77. An appraisal of the frequency and severity of noninfectious manifestations in primary immunodeficiencies: A study of a national retrospective cohort of 1375 patients over 10 years

80. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

81. Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype

82. Symptomatic osteonecrosis in French survivors of Childhood and Adolescent Leukemia: a clinical and radiological study from the L.E.A. program

83. Decision-tree derivation and external validation of a new clinical decision rule (DISCERN-FN) to predict the risk of severe infection during febrile neutropenia in children treated for cancer

84. Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

86. Brothers and sisters of childhood acute leukemia survivors: Their long‐term quality of life and its determinants.

87. Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

88. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options

89. Therapeutic approach and outcome of children with Philadelphia chromosome‐positive acute lymphoblastic leukemia at first relapse in the era of tyrosine kinase inhibitors: An SFCE retrospective study

90. INFECTIOUS DISEASE: Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

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

92. Impact of the social deprivation on the psychosocial difficulties of pediatric cancer survivors: a prospective multicentric study

93. Hydroxychloroquine in mild-to-moderate COVID-19: a placebo-controlled double blind trial

94. Wiskott-Aldrich syndrome

95. Pediatric-Onset Evans Syndrome Is Associated with Broad Immunopathological Manifestations, High Treatment Burden and Mortality in Long-Term Follow-up

96. A syndrome with congenital neutropenia and mutations in G6PC3

97. Hydroxychloroquine in mild-to-moderate coronavirus disease 2019: a placebo-controlled double blind trial

98. Correction to: A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

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

100. Inherited and somatic CD3(sym) mutations in a patient with T-cell deficiency

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