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Journal de Mycologie Médicale, ISSN 1156-5233, 09/2017, Volume 27, Issue 3, pp. e14 - e14
Journal Article
Medecine Therapeutique Pediatrie, ISSN 1286-5494, 2001, Volume 4, Issue 6, pp. 414 - 418
Journal Article
Annales de biologie clinique, 06/2017, Volume 75, Issue 3, p. 348
Streptococcus pneumoniae infections in children are most often lung infections or meningitis. Urinary tract infections are much rarer. We present the case of a... 
Streptococcus pneumoniae - isolation & purification | Urinary Tract Infections - diagnosis | Age Factors | Humans | Pneumococcal Infections - pathology | Child, Preschool | Female | Pneumococcal Infections - diagnosis | Urinary Tract Infections - microbiology
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 2013, Volume 63, Issue 1, pp. 119 - 123
A 20-year-old man was hospitalized for malignant hypertension, mechanical hemolysis, and kidney failure. Kidney biopsy confirmed glomerular and arteriolar... 
Nephrology | MMACHC (methylmalonic aciduria and homocystinuria type C protein) | cobalamin C disease | eculizumab | cobalamin | chronic kidney failure | Hemolytic uremic syndrome (HUS) | HOMOCYSTINURIA CBLC | MICROANGIOPATHY | COMBINED METHYLMALONIC ACIDURIA | DISEASE | DISORDER | UROLOGY & NEPHROLOGY | SPECTRUM | MUTATIONS | MMACHC | Methionine - blood | Recurrence | Kidney - pathology | Amino Acid Metabolism, Inborn Errors - physiopathology | Humans | Male | Leucovorin | Homocystinuria - metabolism | Hydroxocobalamin - administration & dosage | Vitamin B Complex - administration & dosage | Kidney Function Tests | Amino Acid Metabolism, Inborn Errors - diagnosis | Amino Acid Metabolism, Inborn Errors - metabolism | Betaine - administration & dosage | Homocystinuria - physiopathology | Kidney - metabolism | Homocysteine - urine | Amino Acid Metabolism, Inborn Errors - genetics | Antibodies, Monoclonal, Humanized - pharmacology | Adult | Drug Resistance | Kidney - physiopathology | Methylmalonic Acid - urine | Diagnosis, Differential | Homocystinuria - drug therapy | Treatment Outcome | Vitamin B 12 Deficiency - congenital | Carrier Proteins - genetics | Hypertension, Malignant - etiology | Lipotropic Agents - administration & dosage | Biopsy | Mutation | Homocystinuria - diagnosis | Homocystinuria - genetics | Immunologic Factors - pharmacology | Amino Acid Metabolism, Inborn Errors - drug therapy | Renal Dialysis | Immunologic Factors | Hypertension, Malignant | Kidney | Life Sciences | Antibodies, Monoclonal, Humanized | Homocystinuria | Immunology | Betaine | Carrier Proteins | Hydroxocobalamin | Methionine | Amino Acid Metabolism, Inborn Errors | Vitamin B Complex | Lipotropic Agents | Methylmalonic Acid | Homocysteine
Journal Article
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 03/2015, Volume 100, Issue 3, pp. 259 - 264
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 11/2012, Volume 35, Issue 6, pp. 993 - 999
Journal Article
Medical mycology, ISSN 1369-3786, 05/2019
Data on features of Pneumocystis primary infection in infancy are still fragmented. To study Pneumocystis primary infection, 192 infants who were monitored for... 
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 09/2019
The prevalence of neurological involvement in patients with a deletion of or a variant in the HNF1B gene remains discussed. The aim of this study was to... 
Journal Article
Journal Article
Eurosurveillance, ISSN 1025-496X, 02/2019, Volume 24, Issue 8, pp. 35 - 43
Introduction: Haemolytic uraemic syndrome (HUS) related to Shiga toxin-producing Escherichia coli (STEC) is the leading cause of acute renal failure in young... 
O157 | INFECTIOUS DISEASES | INFECTIONS | TRANSMISSION | GROUND-BEEF | RESTRICTION | OUTBREAK | IDENTIFICATION | CHILDREN | Life Sciences | Human health and pathology | Pediatrics | Santé publique et épidémiologie | Infectious diseases | Urology and Nephrology | haemolytic uraemic syndrome | Surveillance | E coli | children | food-borne infections | HUS | Shiga toxin producing Escherichia coli | France
Journal Article
Journal of Nutrition, ISSN 0022-3166, 06/2007, Volume 137, Issue 6, pp. 1561S - 1563S
Hyperphenylalaninemia (HPA) is the most frequently inherited disorder of a mi no acid metabolism (prevalence 1:10,000). In France, a nationwide neonatal... 
NUTRITION & DIETETICS | MUTATIONS | Phenylketonurias - therapy | Monitoring, Physiologic | Phenylketonurias - diagnosis | Humans | Child, Preschool | Phenylalanine - blood | Phenylketonurias - metabolism | Phenylketonurias - urine | Diet Therapy | Child | Phenylketonuria | Care and treatment
Journal Article
Clinical and experimental rheumatology, ISSN 0392-856X, 11/2018, Volume 36, Issue 6, pp. 1103 - 1109
Objective The metacarpophalangeal (MCP) and metatarsophalangeal (MTP) joints may be involved in juvenile idiopathic arthritis. Our goal was to describe their... 
RHEUMATOID-ARTHRITIS | metacarpophalangeal joints | DIAGNOSIS | MANAGEMENT | FINGER JOINTS | JUVENILE IDIOPATHIC ARTHRITIS | physeal cartilage | RHEUMATOLOGY | ultrasound | epiphyseal cartilage | metatarsophalangeal joints | CHILDHOOD ARTHRITIS | DOPPLER ULTRASOUND | healthy children | ULTRASONOGRAPHY | THICKNESS
Journal Article
Seminars in Arthritis and Rheumatism, ISSN 0049-0172, 2011, Volume 41, Issue 2, pp. 272 - 278
Journal Article
Vaccine, ISSN 0264-410X, 2011, Volume 29, Issue 21, pp. 3753 - 3759
Journal Article