Pseudohypoparathyroidism: phenotypic spectrum in kindred

Gelijkaardige items

• Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
  door: Vasanwala, Rashida, et al.
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• Normocalcaemic pseudohypoparathyroidism with unusual phenotype.
  door: Gertner, J M, et al.
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• Neuropsychiatric phenotype in a child with pseudohypoparathyroidism
  door: Visconti, Paola, et al.
  Gepubliceerd in: (2016)
• Right ventricular remodeling and dysfunction among the spectrum of heart failure phenotypes
  door: Wang, Harris, et al.
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• Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation
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