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August 13, 2008The Journal of Clinical Endocrinology & MetabolismOpen Access

Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

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Authors

AGAnthony P. GoldstoneImperial College Healthcare NHS TrustAHAnthony HollandUniversity of CambridgeBHB. P. HauffaEssen University Hospital

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Cite This Study

Goldstone et al. (2008) studied this question.

synapsesocial.com/papers/6a7064256c240de38cdbc907https://doi.org/10.1210/jc.2008-0649
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Maladaptive Behavior Differences in Prader-Willi Syndrome Due to Paternal Deletion Versus Paternal Uniparental Disomy1999 · 180 citations
  2. 2Arousal and Cardiorespiratory Responses to Hypoxia in Prader-Willi Syndrome1996 · 75 citations
  3. 3Impairment of GH responsiveness to combined GH‐releasing hormone and arginine administration in adult patients with Prader‐Willi syndrome2006 · 47 citations
  4. 4Fasting and Postprandial Hyperghrelinemia in Prader-Willi Syndrome Is Partially Explained by Hypoinsulinemia, and Is Not Due to Peptide YY3–36Deficiency or Seen in Hypothalamic Obesity Due to Craniopharyngioma2005 · 117 citations
  5. 5Intracranial abnormalities detected by three‐dimensional magnetic resonance imaging in Prader–Willi syndrome2006 · 95 citations