Note that over the years, PWS has been known as Prader-Willi, Prader-Labhart-Willi or Prader-Willi-Fanconi syndrome, with Prader-Willi syndrome being most commonly used today.
Prader-Willi syndrome (PWS) was first described by Andrea Prader, Alexis Labhart and Heinrich Willi in 1956.
Note that over the years, PWS has been known as Prader-Willi, Prader-Labhart-Willi, or Prader-Willi-Fanconi syndrome, with Prader-Willi syndrome being most commonly used today.
With a genetic condition called Prader-Willi syndrome (PWS).
Has a rare disease called Prader-Willi Syndrome (PWS).
Buiting K. Prader-Willi syndrome and Angelman syndrome.
Rare genetic disorder called Prader-Willi syndrome.
Over the years, the syndrome has been known as Prader-Willi, Prader-Labhart-Willi or Prader-Willi-Fanconi syndrome, with Prader-Willi syndrome being most commonly used today.
for the study of Prader-Willi syndrome and other rare
Inherited diseases: Kalman syndrome, Prader-Willi syndrome and Klinefelter syndrome,
Prader Willi Syndrome was discovered and first diagnosed in 1956 by Swiss doctors Andrea Prader, Alexis Labhart, and Heinrich Willi.
Harvey is blind, autistic and has condition called Prader Willi Syndrome.
Endocrine disorders such as Cushing’s Syndrome and Prader Willi Syndrome
There are generally two stages of symptoms for people with Prader-Willi syndrome:
Genetic disorders, such as Prader-Willi syndrome, familial diabetes insipidus, Kallmann syndrome
There is a host of information on the Internet about Prader-Willi syndrome.
If you have Prader-Willi syndrome (a chromosomal disorder).
Examples include Prader-Willi syndrome and Angelman syndrome.
My third child, Brooke, has Prader-Willi Syndrome.
If the patient has Prader-Willi syndrome (a chromosomal disorder).
Prader-Willi syndrome (PWS), for improvement of growth and body composition.
Prader-Willi syndrome (PWS), for improvement of growth and body composition.
Prader-Willi syndrome is difficult to manage in the home.
This invention relates to treating Prader-Willi Syndrome (PWS) using a KATP channel opener.
Growth disorder in Prader-Willi syndrome, with the aim of improving the growth and structure of the body.
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