Thomas J Neuhaus


Ontology type: schema:Person     


Person Info

NAME

Thomas J

SURNAME

Neuhaus

Publications in SciGraph latest 50 shown

  • 2018-02 Acute regulated expression of pendrin in human urinary exosomes in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2017-05 Long-term health-related quality of life and psychological adjustment in children after haemolytic-uraemic syndrome in PEDIATRIC NEPHROLOGY
  • 2016-06 Health-related quality of life and mental health in parents of children with hemolytic uremic syndrome in PEDIATRIC NEPHROLOGY
  • 2016-06 Erratum to: Health-related quality of life and mental health in parents of children with hemolytic uremic syndrome in PEDIATRIC NEPHROLOGY
  • 2016-05 Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract in EUROPEAN JOURNAL OF PEDIATRICS
  • 2015-09 Hochspezialisierte Medizin in der Schweiz: Sicht des Kinderspitals Luzern in PÄDIATRIE & PÄDOLOGIE
  • 2015-03 Neurodevelopmental long-term outcome in children after hemolytic uremic syndrome in PEDIATRIC NEPHROLOGY
  • 2013-07 Successful long-term outcome after renal transplantation in a patient with atypical haemolytic uremic syndrome with combined membrane cofactor protein CD46 and complement factor I mutations in PEDIATRIC NEPHROLOGY
  • 2012-12 Long lasting efficacy of sorafenib in a heavily pretreated patient with thymic carcinoma in TARGETED ONCOLOGY
  • 2012-11 Successful treatment of intractable hiccups by oral application of lidocaine in SUPPORTIVE CARE IN CANCER
  • 2012-07 Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver disease in PEDIATRIC NEPHROLOGY
  • 2012-03 Weight dosing of steroids in nephrotic syndrome in PEDIATRIC NEPHROLOGY
  • 2011-03 TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum in NATURE GENETICS
  • 2011-02 Recurrence of membranoproliferative glomerulonephritis after renal transplantation in Denys–Drash in PEDIATRIC NEPHROLOGY
  • 2010 Komplexe Gerinnungsstörungen in HÄMOSTASEOLOGIE
  • 2009-07 Intellectual and motor performance, quality of life and psychosocial adjustment in children with cystinosis in PEDIATRIC NEPHROLOGY
  • 2009-01 A phase III trial of topotecan and whole brain radiation therapy for patients with CNS-metastases due to lung cancer in BRITISH JOURNAL OF CANCER
  • 2008-09 A boy with congenital analbuminemia and steroid-sensitive idiopathic nephrotic syndrome: an experiment of nature in EUROPEAN JOURNAL OF PEDIATRICS
  • 2008-09 Randomised trial of oral versus sequential intravenous/oral cephalosporins in children with pyelonephritis in EUROPEAN JOURNAL OF PEDIATRICS
  • 2008-08 Outcome after renal transplantation. Part I: Intellectual and motor performance in PEDIATRIC NEPHROLOGY
  • 2008-08 Outcome after renal transplantation. Part II: Quality of life and psychosocial adjustment in PEDIATRIC NEPHROLOGY
  • 2008-08 Metabolic and orthopedic management of X-linked vitamin D-resistant hypophosphatemic rickets in JOURNAL OF CHILDREN'S ORTHOPAEDICS
  • 2008-03 Inherited renal tubular dysgenesis: the first patients surviving the neonatal period in EUROPEAN JOURNAL OF PEDIATRICS
  • 2007-12 Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis in KIDNEY INTERNATIONAL
  • 2007-11 Selective late steroid withdrawal after renal transplantation in PEDIATRIC NEPHROLOGY
  • 2007-03 Obesity and other clinical endpoints in steroid-sensitive nephrotic syndrome in PEDIATRIC NEPHROLOGY
  • 2006-12 Hyperuricemia and gout following pediatric renal transplantation in PEDIATRIC NEPHROLOGY
  • 2006-10 Loss of imprinting of the insulin-like growth factor 2 and the H19 gene in testicular seminomas detected by real-time PCR approach in ARCHIVES OF TOXICOLOGY
  • 2006-07 Living-related kidney transplantation in pediatric recipients in PEDIATRIC NEPHROLOGY
  • 2006-03 Transplantation of infant en bloc kidneys into paediatric recipients in PEDIATRIC NEPHROLOGY
  • 2005-09 Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis in NATURE GENETICS
  • 2005-03 Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD) in KIDNEY INTERNATIONAL
  • 2005-02 Psychosocial impact of living-related kidney transplantation on donors and partners in PEDIATRIC NEPHROLOGY
  • 2004-12 Immunization in children with chronic renal failure: a practical approach in PEDIATRIC NEPHROLOGY
  • 2004-08 Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome in KIDNEY INTERNATIONAL
  • 2004-07 Reliability of non-invasively acquired human genomic DNA as a substrate for real-time PCR-assisted analysis of genetic polymorphisms in ARCHIVES OF TOXICOLOGY
  • 2004-02 Recovery of renal function after long-term dialysis in hemolytic uremic syndrome in PEDIATRIC NEPHROLOGY
  • 2003-07 An 11-month-old boy with psychomotor regression and auto-aggressive behaviour in EUROPEAN JOURNAL OF PEDIATRICS
  • 2003-03 Severe acute abdominal pain in idiopathic nephrotic syndrome in PEDIATRIC NEPHROLOGY
  • 2002-11 Influence of family structure on course of steroid-sensitive nephrotic syndrome in PEDIATRIC NEPHROLOGY
  • 2002-10 Cardiac rhythm disturbances in children on hemodialysis in PEDIATRIC NEPHROLOGY
  • 2002-08 Immunization in children with chronic renal failure in PEDIATRIC NEPHROLOGY
  • 2002-04 The Ets 1 transcription factor is upregulated during inflammatory angiogenesis in rheumatoid arthritis in JOURNAL OF MOLECULAR MEDICINE
  • 2002-03 Hyperammonaemic encephalopathy in a 13-year-old boy in EUROPEAN JOURNAL OF PEDIATRICS
  • 2001-02 Simultaneous occurrence of the haemolytic uraemic syndrome and acute post-infectious glomerulonephritis in EUROPEAN JOURNAL OF PEDIATRICS
  • 2000-07 Heparin-induced thrombocytopenia type II on hemodialysis: switch to danaparoid in PEDIATRIC NEPHROLOGY
  • 2000-06 Rapid analysis of α1-antitrypsin PiZ genotype by a real-time PCR approach in JOURNAL OF MOLECULAR MEDICINE
  • 1999-06 Familial syndrome of infantile polycythemia with markedly elevated erythropoietin, severe pulmonary hypertension, and intrapulmonary hematopoiesis - an “inappropriate” hypoxic response? in PEDIATRIC RESEARCH
  • 1998-12 A 14-month-old boy with cardiomegaly and heart failure in EUROPEAN JOURNAL OF PEDIATRICS
  • 1998-06 Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations in KIDNEY INTERNATIONAL
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