Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children

[1]  G. Diaz,et al.  Ocular disease in the cobalamin C defect: a review of the literature and a suggested framework for clinical surveillance. , 2015, Molecular genetics and metabolism.

[2]  M. Baumgartner,et al.  Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancy , 2014, Orphanet Journal of Rare Diseases.

[3]  Shuohua Chen,et al.  Homocysteine as a Risk Factor for Hypertension: A 2-Year Follow-Up Study , 2014, PloS one.

[4]  Z. Bobby,et al.  Hyperhomocysteinemia, Insulin Resistance and High HS- CRP Levels in Prehypertension. , 2014, Journal of clinical and diagnostic research : JCDR.

[5]  M. Baumgartner,et al.  Clinical presentation and outcome in a series of 88 patients with the cblC defect , 2014, Journal of Inherited Metabolic Disease.

[6]  V. García-Nieto,et al.  Aciduria metilmalónica con homocistinuria: una causa muy poco frecuente de fallo renal en el período neonatal , 2014 .

[7]  M. Roy,et al.  Long-term visual outcome of methylmalonic aciduria and homocystinuria, cobalamin C type. , 2014, Ophthalmology.

[8]  Mónica Ruiz-Pons,et al.  Methylmalonic acidemia with homocystinuria. A very rare cause of kidney failure in the neonatal period. , 2014, Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia.

[9]  T. Naidich,et al.  Neurologic and neurodevelopmental phenotypes in young children with early-treated combined methylmalonic acidemia and homocystinuria, cobalamin C type. , 2013, Molecular genetics and metabolism.

[10]  A. Losito,et al.  Combined Pulmonary Hypertension and Renal Thrombotic Microangiopathy in Cobalamin C Deficiency , 2013, Pediatrics.

[11]  X. Gu,et al.  [Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment]. , 2013, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[12]  S. Kölker,et al.  Metabolic decompensation in methylmalonic aciduria: which biochemical parameters are discriminative? , 2012, Journal of Inherited Metabolic Disease.

[13]  C. Venditti,et al.  Combined methylmalonic acidemia and homocystinuria, cblC type. II. Complications, pathophysiology, and outcomes , 2012, Journal of Inherited Metabolic Disease.

[14]  R. Chandler,et al.  Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management , 2012, Journal of Inherited Metabolic Disease.

[15]  Zhixian Yang,et al.  Epilepsy in children with methylmalonic acidemia: Electroclinical features and prognosis , 2011, Brain and Development.

[16]  W. Tu.  Methylmalonic Acidemia in Mainland China , 2011, Annals of Nutrition and Metabolism.

[17]  V. Frémeaux-Bacchi,et al.  Atypical hemolytic uremic syndrome , 2011, Orphanet journal of rare diseases.

[18]  G. Salomons,et al.  CD46-associated atypical hemolytic uremic syndrome with uncommon course caused by cblC deficiency , 2010, Pediatric Nephrology.

[19]  G. Diaz,et al.  Newborn screening and early biochemical follow-up in combined methylmalonic aciduria and homocystinuria, cblC type, and utility of methionine as a secondary screening analyte. , 2010, Molecular genetics and metabolism.

[20]  J. Groothoff,et al.  Prophylactic plasma exchange in CD46-associated atypical haemolytic uremic syndrome , 2009, Pediatric Nephrology.

[21]  X. Gu,et al.  [Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia]. , 2009, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[22]  C. Greenberg,et al.  Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder , 2007, Pediatric Nephrology.

[23]  Yuehua Zhang,et al.  [Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia]. , 2007, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[24]  J. Saudubray,et al.  Branched-chain organic acidurias. , 2002, Seminars in neonatology : SN.