Home
About
Overview
Sharing Data
ORCID
Help
History (14)
Continuous paravertebral extrapleural infusion for post-thoracotomy pain management.
Pathophysiology of blood-brain barrier breakdown.
Hemoglobin stability in patients with anemia, CKD, and type 2 diabetes: an analysis of the TREAT (Trial to Reduce Cardiovascular Events With Aranesp Therapy) placebo arm.
Changes in mRNA and protein levels of proteoglycans of the anulus fibrosus and nucleus pulposus during intervertebral disc degeneration.
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?
See All 14 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis? Indian J Pediatr. 2013 Aug; 80(8):688-90.
View in:
PubMed
subject areas
Chromosomes, Human, Pair 4
DNA Repeat Expansion
Female
Homeodomain Proteins
Humans
Hypoventilation
Infant, Newborn
Sleep Apnea, Central
Transcription Factors
authors with profiles
Elizabeth Berry-Kravis