Japanese
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

pseudohypoparathyroidism/headache

リンクがクリップボードに保存されます
5 結果

Bilateral, symmetrical and extensive cerebral calcification in pseudohypoparathyroidism.

登録ユーザーのみが記事を翻訳できます
ログインサインアップ
Pseudohypoparathyroidism (PHP) is a heterogeneous group of disorders characterized by hypocalcemia, hyperphosphatemia, increased serum concentration of parathyroid hormone (PTH), and insensitivity to the biological activity of PTH. Pseudohypoparathyroidism is rare sporadic or autosomal dominant

Visual disturbances as a presenting feature of pseudohypoparathyroidism.

登録ユーザーのみが記事を翻訳できます
ログインサインアップ
BACKGROUND Visual disturbance as a presenting feature of pseudohypoparathyroidism (PHP) is uncommon. Although papilledema is commonly reported with hypoparathyroidism primary or secondary, but not reported commonly with PHP. METHODS A 10-year-old male child presented to our outpatient service with

Plurihormone secreting pituitary macroadenoma masquerading as thyrotoxicosis: Clinical presentation and diagnostic challenges.

登録ユーザーのみが記事を翻訳できます
ログインサインアップ
Thyroid stimulating hormone (TSH) secreting adenomas are the rarest type of pituitary adenomas (1:1000000 in the population; 0.2- 2.8% of adenomas). Plurihormonal thyrotropic adenomas are even rarer usually having cosecretion of growth hormone (GH) and prolactin. We report perhaps for the first

Fahr's syndrome in Southern Tunisia: A broad spectrum of clinical and etiological features.

登録ユーザーのみが記事を翻訳できます
ログインサインアップ
OBJECTIVE We describe the clinical and etiological profile of patients with Fahr's syndrome (FS). METHODS Charts of sixteen patients diagnosed with FS between 1999 and 2014 were retrospectively assessed. RESULTS The mean age at diagnosis was 44.68 years (11-67 years). The most main presenting

Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes.

登録ユーザーのみが記事を翻訳できます
ログインサインアップ
There are now a number genes, known to be associated with familial primary brain calcification (PFBC), causing the so called 'Fahr's' disease or syndrome. These are SCL20A2, PDGFB, PDGFRB and XPR1. In this systematic review, we analyse the clinical and radiological features reported in genetically
Facebookページに参加する

科学に裏打ちされた最も完全な薬草データベース

  • 55の言語で動作します
  • 科学に裏打ちされたハーブ療法
  • 画像によるハーブの認識
  • インタラクティブGPSマップ-場所にハーブをタグ付け(近日公開)
  • 検索に関連する科学出版物を読む
  • それらの効果によって薬草を検索する
  • あなたの興味を整理し、ニュース研究、臨床試験、特許について最新情報を入手してください

症状や病気を入力し、役立つ可能性のあるハーブについて読み、ハーブを入力して、それが使用されている病気や症状を確認します。
*すべての情報は公開された科学的研究に基づいています

Google Play badgeApp Store badge