Update Pediatric Reference: Failure To Thrive in Children

  • Interprofessional group intervention for parents of children age 3 and younger with feeding difficulties: pilot program evaluation.
    Owen C, et al. Nutr Clin Pract. 2012
  • Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
    Shoukier M, et al. Clin Genet. 2012
  • [Obstructive sleep apnea in childhood : Anesthesiological aspects].
    Schnoor J, et al. Anaesthesist. 2012.
  • Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly.
    Tasic V, et al. Pediatr Nephrol. 2011
  • Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.
    Grünert SC, et al. Mol Genet Metab. 2011
  • Gastrointestinal Endoscopy and Mucosal Biopsy in the First Year of Life: Indications and Outcome.
    Volonaki E, et al. J Pediatr Gastroenterol Nutr. 2011
  • Development of a risk-stratification tool for medical child abuse in failure to thrive.
    Mash C, et al. Pediatrics. 2011
  • Failure to thrive in infants with complicated facial hemangiomas.
    Thomas MW, et al. Pediatr Dermatol. 2012
    Vitamin B12 deficiency in a 9-month-old boy.
    Quentin C, et al. Eur J Pediatr. 2012
  • Inflammatory bowel disease in children, an evolving problem in Kuwait.
    Al-Qabandi WA, et al. Saudi J Gastroenterol. 2011
  • Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.
    Hubert EL, et al. J Am Soc Nephrol. 2011
  • Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
    Jacquemont S, et al. Nature. 2011
  • HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome.
    Niihori T, et al. J Hum Genet. 2011
  • Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome.
    Gripp KW, et al. Am J Med Genet A. 2011
  • Cryptosporidium infection in patients with major histocompatibility complex class II deficiency syndrome in Tunisia: description of five cases].
    Ben Abda I, et al. Arch Pediatr. 2011.
  • Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?
    Jain-Ghai S, et al. Mol Genet Metab. 2011
  • Serological screening for celiac disease in symptomatic 12 to 36 month-old children.
    Modelli IC, et al. Arq Gastroenterol. 2010
  • Costello Syndrome.
    Gripp KW, et al. GeneReviews. 1993
    Free full text
    Citrin Deficiency.
    Kobayashi K, et al. GeneReviews. 1993
  • Transcobalamin (TC) deficiency–potential cause of bone marrow failure in childhood.
    Prasad C, et al. J Inherit Metab Dis. 2008

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