about
AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosisHemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experience.Eculizumab therapy for atypical haemolytic uraemic syndrome due to a gain-of-function mutation of complement factor B.Does dysregulated complement activation contribute to haemolytic uraemic syndrome secondary to Streptococcus pneumoniae?Eculizumab in atypical haemolytic uraemic syndrome with severe cardiac and neurological involvement.Factors influencing success of clinical genome sequencing across a broad spectrum of disordersSimultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylationMutations in PIK3R1 cause SHORT syndromeChildren with nephrotic syndrome have greater bone area but similar volumetric bone mineral density to healthy controlsTolvaptan treatment for severe neonatal autosomal-dominant polycystic kidney disease.Patients' and health-care professionals' awareness of cost: a multicentre survey.Diabetes and nephrotic syndrome: Answers.Diabetes and nephrotic syndrome: Questions.Cisplatin-induced haemolytic uraemic syndrome associated with a novel intronic mutation of CD46 treated with eculizumabProgressive myoclonic epilepsy with Fanconi syndrome.Urinary L-lactate excretion is increased in renal Fanconi syndrome.Exome analysis resolves differential diagnosis of familial kidney disease and uncovers a potential confounding variant.The clinical course of hepatitis B virus-associated nephropathy.Pearson's syndrome presenting with Fanconi syndrome.Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.Patient with an EYA1 mutation with features of branchio-oto-renal and oto-facio-cervical syndrome.Acute renal failure in a patient with paroxysmal cold hemoglobinuria.Basal metabolic rate in children with chronic kidney disease and healthy control children.Acute promyelocytic leukemia. A childhood cluster.Professionals Against Child Abuse express support for David Southall.Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosisMyocardial infarction in Kawasaki diseaseInteraction between clonidine and cyclosporine AAbdominal aortic aneurysms in childrenStreptococcus pneumoniae-associated hemolytic uremic syndromeBilateral multicystic kidneys--an unusual caseRituximab therapy for steroid-dependent minimal change nephrotic syndromeLaparoscopic renal biopsy in obese childrenVitamin B6 in Pediatric Renal Transplant Recipients
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Rodney D Gilbert
@es
Rodney D. Gilbert
@en
Rodney D. Gilbert
@sl
رودني دي. غيلبرت
@ar
type
label
Rodney D Gilbert
@es
Rodney D. Gilbert
@en
Rodney D. Gilbert
@sl
رودني دي. غيلبرت
@ar
prefLabel
Rodney D Gilbert
@es
Rodney D. Gilbert
@en
Rodney D. Gilbert
@sl
رودني دي. غيلبرت
@ar
P106
P1153
7401932319
P21
P31
P496
0000-0001-7426-0188
P569
2000-01-01T00:00:00Z