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Pegvisomant treatment in a 4-year-old girl with neurofibromatosis type 1
Katharina M Main
,
Astrid Sehested
,
Ulla Feldt-Rasmussen
17
Citationer (Scopus)
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Keyphrases
4-year-olds
100%
Pegvisomant
100%
Neurofibromatosis Type I
100%
Neurofibromatosis Type 1 (NF-1)
100%
Standard Deviation Score
60%
Growth Hormone Deficiency
60%
Insulin-like Growth factor-1
40%
Insulin-like Growth Factor Binding protein-3 (IGFBP-3)
40%
Treatment Duration
20%
AIMS™
20%
Long-term Treatment
20%
Visual Impairment
20%
Fasting Plasma Glucose
20%
Three-level
20%
Current Treatment
20%
Treatment Options
20%
Thyroid Function
20%
Glycated Hemoglobin
20%
Rare Disorders
20%
Adrenal Function
20%
Somatostatin Analogs
20%
Octreotide
20%
Height Standard Deviation Score
20%
Gonadal Function
20%
Intracranial Tumor
20%
Non-fasting
20%
Serum Growth Hormone
20%
Growth Velocity
20%
Catch-up Growth
20%
Height Velocity
20%
Growth Hormone Receptor Antagonist
20%
Target Height
20%
Repeat Test
20%
Pituitary Surgery
20%
Pituitary Radiotherapy
20%
Optic Pathway Glioma
20%
Medicine and Dentistry
Pegvisomant
100%
Neurofibromatosis Type I
100%
Growth Hormone
80%
Side Effect
40%
Visual Impairment
20%
Blood Glucose
20%
Glycated Hemoglobin
20%
Orphan Disorder
20%
Adrenal Function
20%
Growth Rate
20%
Octreotide
20%
Somatostatin Derivative
20%
Thyroid Function
20%
Acromegaly
20%
Gonad Function
20%
Growth Hormone Receptor
20%
Hormone Receptor Blocking Agent
20%
Intracranial Tumor
20%
Pituitary Surgery
20%
Optic Nerve Glioma
20%
Pharmacology, Toxicology and Pharmaceutical Science
Pegvisomant
100%
Neurofibromatosis Type 1
100%
Growth Hormone
80%
Side Effect
40%
Disease
20%
Visual Impairment
20%
Glycosylated Hemoglobin
20%
Hormone Receptor Blocking Agent
20%
Acromegaly
20%
Octreotide
20%
Somatostatin Derivative
20%
Growth Hormone Receptor
20%
Intracranial Tumor
20%
Optic Nerve Glioma
20%