Detalhe da pesquisa
1.
Individual and Family Determinants for Quality of Life in Parents of Children with Inborn Errors of Metabolism Requiring a Restricted Diet: A Multilevel Analysis Approach.
J Pediatr
; 254: 39-47.e4, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36265570
2.
Determinants of Quality of Life in Children with Inborn Errors of Metabolism Receiving a Restricted Diet.
J Pediatr
; 242: 192-200.e3, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34788681
3.
Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.
Kidney Int
; 99(3): 737-749, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32750455
4.
Health Status of French Young Patients with Inborn Errors of Metabolism with Lifelong Restricted Diet.
J Pediatr
; 220: 184-192.e6, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32145964
5.
Pneumocystis primary infection in infancy: Additional French data and review of the literature.
Med Mycol
; 58(2): 163-171, 2020 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31127850
6.
Treatment and outcome of congenital nephrotic syndrome.
Nephrol Dial Transplant
; 34(3): 458-467, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29474669
7.
Normal sonoanatomy of small joints in healthy children: changes in cartilage and vascularisation according to age and gender.
Clin Exp Rheumatol
; 36(6): 1103-1109, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30148439
8.
Normal sonoanatomy of the paediatric entheses including echostructure and vascularisation changes during growth.
Eur Radiol
; 25(7): 2143-52, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25663311
9.
Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.
Am J Kidney Dis
; 63(1): 119-23, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24210589
10.
Pneumocystis Is Still Involved in Nonimmunosuppressed Preterm Infants in Europe.
Clin Infect Dis
; 67(4): 645-646, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29462273
11.
Efficacy and safety of BH4 before the age of 4 years in patients with mild phenylketonuria.
J Inherit Metab Dis
; 35(6): 975-81, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22388642
12.
Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation.
J Inherit Metab Dis
; 35(6): 993-9, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22669364
13.
Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.
EBioMedicine
; 51: 102623, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31923802
14.
School level of children carrying a HNF1B variant or a deletion.
Eur J Hum Genet
; 28(1): 56-63, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31481685
15.
Streptococcus pneumoniae urinary tract infection in pedeatrics.
Ann Biol Clin (Paris)
; 75(3): 348-350, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28540858
16.
[Recommendations for management of patients from pediatrics unit to adult unit: Transition and transfer program]. / Transition et transfert de la néphrologie pédiatrique à la néphrologie adulte : recommandations de la filière maladies rénales rares ORKiD.
Nephrol Ther
; 17(2): 137-142, 2021 04.
Artigo
em Francês
| MEDLINE | ID: mdl-33531259
17.
18.
Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.
Arch Dis Child
; 100(3): 259-64, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25324567
19.
Genotype-phenotype associations in French patients with phenylketonuria and importance of genotype for full assessment of tetrahydrobiopterin responsiveness.
Orphanet J Rare Dis
; 10: 158, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26666653
20.
Imaging approaches for evaluating peripheral joint abnormalities in juvenile idiopathic arthritis.
Semin Arthritis Rheum
; 41(5): 698-711, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22035628