An unusual cause of hypertension with hematuria and proteinuria: Questions

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Pediatric nephrology (Berlin, West)

• Publication date

  2016-03-15

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s00467-016-3344-2PMID 26980088
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• An international consensus approach to the management of atypical hemolytic uremic syndrome in children

  2015cited by this paper
• Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data

  2015cited by this paper
• Adult-onset renal thrombotic microangiopathy and pulmonary arterial hypertension in cobalamin C deficiency.

  2015cited by this paper
• Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines

  2015cited by this paper
• Nephrotic syndrome and thrombotic microangiopathy caused by cobalamin C deficiency

  2015cited by this paper
• Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.

  2014cited by this paper
• Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy

  2014cited by this paper
• Atypical glomerulopathy associated with the cblE inborn error of vitamin B12 metabolism

  2013cited by this paper
• Combined Pulmonary Hypertension and Renal Thrombotic Microangiopathy in Cobalamin C Deficiency

  2013cited by this paper
• Lessons in biology from patients with inborn errors of vitamin B12 metabolism.

  2013cited by this paper
• cblE-Type Homocystinuria Presenting with Features of Haemolytic-Uremic Syndrome in the Newborn Period.

  2012cited by this paper
• Inborn errors of cobalamin absorption and metabolism

  2011cited by this paper
• CD46-associated atypical hemolytic uremic syndrome with uncommon course caused by cblC deficiency

  2010cited by this paper
• Long-term outcome in methylmalonic aciduria: a series of 30 French patients.

  2009cited by this paper
• Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder

  2007cited by this paper
• Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation.

  2005cited by this paper
• Homocysteine Increases the Expression of Vascular Endothelial Growth Factor by a Mechanism Involving Endoplasmic Reticulum Stress and Transcription Factor ATF4*

  2004cited by this paper
• Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period.

  2002cited by this paper
• Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.

  2002cited by this paper
• Cobalamin C deficiency complicated by an atypical glomerulopathy

  2002cited by this paper
• Homocysteine-induced endoplasmic reticulum stress and growth arrest leads to specific changes in gene expression in human vascular endothelial cells.

  1999cited by this paper
• Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency

  1999cited by this paper
• Tissue Plasminogen Activator Binding to the Annexin II Tail Domain

  1998cited by this paper
• Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

  1996cited by this paper
• Association between plasma homocysteine concentrations and extracranial carotid-artery stenosis.

  1995cited by this paper
• Homocysteine, a risk factor for premature vascular disease and thrombosis, induces tissue factor activity in endothelial cells.

  1993cited by this paper
• A congenital anomaly of vitamin B12 metabolism: a study of three cases.

  1992cited by this paper
• Cobalamin C defect associated with hemolytic-uremic syndrome.

  1992cited by this paper
• Inhibition of thrombomodulin surface expression and protein C activation by the thrombogenic agent homocysteine.

  1991cited by this paper
• Activation of endogenous factor V by a homocysteine-induced vascular endothelial cell activator.

  1986cited by this paper

• Megaloblastic Anemia Progressing to Severe Thrombotic Microangiopathy in Patients with Disordered Vitamin B12 Metabolism: Case Reports and Literature Review.

  2018cites this paper
• A child presenting with severe hypertension and circulatory failure, a diagnostic conundrum: Questions

  2017cites this paper
• Renal thrombotic microangiopathy and pulmonary arterial hypertension in a patient with late-onset cobalamin C deficiency

  2017cites this paper