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Acromegaly and pituitary gigantism
Growth hormone
Haemochromatosis
Hyperthyroidism
Hypophyseal
Hypothyroidism
Insufficiency NOS
Pituitary
Pituitary activity
Pituitary gigantism
Pituitary gland
Pituitary gland-related
Pituitary hormone
Pituitary-adrenal axis
Sheehan's syndrome Simmonds' disease
Short stature
Thyrotoxicosis

Vertaling van "Pituitary gigantism " (Engels → Nederlands) :

Pituitary gigantism

gigantisme door overmaat aan groeihormoon


Acromegaly and pituitary gigantism

acromegalie en hypofysair gigantisme


Arthropathy in:acromegaly and pituitary gigantism (E22.0+) | haemochromatosis (E83.1+) | hypothyroidism (E00-E03+) | thyrotoxicosis [hyperthyroidism] (E05.-+) |

artropathie bij | acromegalie en hypofysair gigantisme (E22.0) | artropathie bij | hemochromatose (E83.1) | artropathie bij | hypothyroïdie (E00-E03) | artropathie bij | thyrotoxicose [hyperthyroïdie] (E05.-)




Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease

dwerggroei van Lorain-Levi | fertiel eunuchoïdisme | geïsoleerde deficiëntie van | ACTH | geïsoleerde deficiëntie van | gonadotropine | geïsoleerde deficiëntie van | groeihormoon | geïsoleerde deficiëntie van | hypofysair hormoon | hypofysaire | cachexie | hypofysaire | insufficiëntie NNO | hypofysaire | kleine gestalte | hypogonadotroop hypogonadisme | idiopathische groeihormoondeficiëntie | necrose van hypofyse (post partum) | panhypopituïtarisme | syndroom van Kallmann | syndroom van Sheehan | ziekte van Simmonds


Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t

gecombineerde hypofysehormoondeficiënties, genetische vormen


A type of central congenital hypothyroidism with characteristics of low levels of thyroid hormones due to insufficient release of thyroid-stimulating hormone (TSH) caused by pituitary resistance to thyrotropin-releasing hormone (TRH). It may or may n

congenitale centrale hypothyreoïdie door deficiëntie van thyrotropine-'releasing'-hormoonreceptor




pituitary activity

werkzaamheid van de hypofyse | werkzaamheid van de pijnappelklier


hypophyseal | pituitary gland-related

hypofysair | met betrekking tot het hersenaanhangsel




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Date index: 2022-10-05
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