- Heřmanský–
Pudlák syndrome (often
written Hermansky–
Pudlak syndrome or
abbreviated HPS) is an
extremely rare
autosomal recessive disorder which results...
- Hermansky–
Pudlak syndrome 1
protein is a
protein that in
humans is
encoded by the HPS1 gene. This gene
encodes a
protein that may play a role in organelle...
-
results in
pigmentary abnormalities and
immune system dysfunction. Hermansky-
Pudlak syndrome: A rare
genetic disorder causing albinism,
bleeding disorders,...
-
Oculocutaneous albinism is a form of
albinism involving the eyes (oculo-), the skin (-cutaneous), and the hair. Overall, an
estimated 1 in 20,000 people...
- is. A
strong form of the
second incompleteness theorem,
proved by
Pavel Pudlák, who was
building on
earlier work by
Solomon Feferman,
states that no consistent...
- applications. Australia: Thomson/Course Technology. ISBN 978-0-619-21558-3.
Pudlák,
Pavel (2013). "Mathematical structures".
Logical foundations of mathematics...
- and was
written up by Solovay,
Reinhardt &
Kanamori (1978).
According to
Pudlák (2013, p. 204), Vopěnka's
principle was
originally intended as a joke: Vopěnka...
- fibrosis[1],
chronic kidney disease,
idiopathic pulmonary fibrosis, Hermansky-
Pudlak syndrome pulmonary fibrosis, skin fibrosis, and
metabolic disorders such...
- However,
currently only
conditional negative results are known. Krajíček and
Pudlák (1998)
proved that
Extended Frege is not
weakly automatable unless RSA is...
- Hermansky–
Pudlak syndrome 5
protein is a
protein that in
humans is
encoded by the HPS5 gene. This gene
encodes a
protein that may play a role in organelle...
