These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 11343310)

  • 1. Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome.
    Weese-Mayer DE; Silvestri JM; Huffman AD; Smok-Pearsall SM; Kowal MH; Maher BS; Cooper ME; Marazita ML
    Am J Med Genet; 2001 May; 100(3):237-45. PubMed ID: 11343310
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome.
    Marazita ML; Maher BS; Cooper ME; Silvestri JM; Huffman AD; Smok-Pearsall SM; Kowal MH; Weese-Mayer DE
    Am J Med Genet; 2001 May; 100(3):229-36. PubMed ID: 11343309
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulation.
    Weese-Mayer DE; Berry-Kravis EM; Ceccherini I; Rand CM
    Respir Physiol Neurobiol; 2008 Dec; 164(1-2):38-48. PubMed ID: 18579454
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.
    Weese-Mayer DE; Berry-Kravis EM; Zhou L; Maher BS; Silvestri JM; Curran ME; Marazita ML
    Am J Med Genet A; 2003 Dec; 123A(3):267-78. PubMed ID: 14608649
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pupillometry in congenital central hypoventilation syndrome (CCHS): quantitative evidence of autonomic nervous system dysregulation.
    Patwari PP; Stewart TM; Rand CM; Carroll MS; Kuntz NL; Kenny AS; Brogadir CD; Weese-Mayer DE
    Pediatr Res; 2012 Mar; 71(3):280-5. PubMed ID: 22278185
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.
    Gronli JO; Santucci BA; Leurgans SE; Berry-Kravis EM; Weese-Mayer DE
    Pediatr Pulmonol; 2008 Jan; 43(1):77-86. PubMed ID: 18041756
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.
    Weese-Mayer DE; Bolk S; Silvestri JM; Chakravarti A
    Am J Med Genet; 2002 Feb; 107(4):306-10. PubMed ID: 11840487
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Developmental disorders affecting the respiratory system: CCHS and ROHHAD.
    Ceccherini I; Kurek KC; Weese-Mayer DE
    Handb Clin Neurol; 2022; 189():53-91. PubMed ID: 36031316
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autism spectrum disorder in young patients with congenital central hypoventilation syndrome: role of the autonomic nervous system dysfunction.
    Dudoignon B; Maruani A; Delorme R; Patout M; Fefeu M; Ellul P; Bokov P; Delclaux C
    Orphanet J Rare Dis; 2024 Jul; 19(1):249. PubMed ID: 38961480
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in
    Spielmann M; Hernandez-Miranda LR; Ceccherini I; Weese-Mayer DE; Kragesteen BK; Harabula I; Krawitz P; Birchmeier C; Leonard N; Mundlos S
    J Med Genet; 2017 Nov; 54(11):754-761. PubMed ID: 28779001
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Idiopathic congenital central hypoventilation syndrome: the next generation.
    Silvestri JM; Chen ML; Weese-Mayer DE; McQuitty JM; Carveth HJ; Nielson DW; Borowitz D; Cerny F
    Am J Med Genet; 2002 Sep; 112(1):46-50. PubMed ID: 12239719
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.
    Weese-Mayer DE; Rand CM; Berry-Kravis EM; Jennings LJ; Loghmanee DA; Patwari PP; Ceccherini I
    Pediatr Pulmonol; 2009 Jun; 44(6):521-35. PubMed ID: 19422034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome.
    Weese-Mayer DE; Berry-Kravis EM; Marazita ML
    Respir Physiol Neurobiol; 2005 Nov; 149(1-3):73-82. PubMed ID: 16054879
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital central hypoventilation syndrome (CCHS): Circadian temperature variation.
    Saiyed R; Rand CM; Carroll MS; Koliboski CM; Stewart TM; Brogadir CD; Kenny AS; Petersen EK; Carley DW; Weese-Mayer DE
    Pediatr Pulmonol; 2016 Mar; 51(3):300-7. PubMed ID: 26086998
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autonomic function in children with congenital central hypoventilation syndrome and their families.
    O'Brien LM; Holbrook CR; Vanderlaan M; Amiel J; Gozal D
    Chest; 2005 Oct; 128(4):2478-84. PubMed ID: 16236912
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A nonverbal learning disability in a case of central hypoventilation syndrome without a PHOX2B gene mutation.
    Trobliger R; Zaroff CM; Grayson RH; Higgins JJ
    Child Neuropsychol; 2010; 16(2):202-8. PubMed ID: 19813116
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital central hypoventilation syndrome: Broader cognitive deficits revealed by parent controls.
    Zelko FA; Stewart TM; Brogadir CD; Rand CM; Weese-Mayer DE
    Pediatr Pulmonol; 2018 Apr; 53(4):492-497. PubMed ID: 29327497
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children.
    Charnay AJ; Antisdel-Lomaglio JE; Zelko FA; Rand CM; Le M; Gordon SC; Vitez SF; Tse JW; Brogadir CD; Nelson MN; Berry-Kravis EM; Weese-Mayer DE
    Chest; 2016 Mar; 149(3):809-15. PubMed ID: 26378991
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurogenic hypertension characterizes children with congenital central hypoventilation syndrome and is aggravated by alveolar hypoventilation during sleep.
    Dudoignon B; Bokov P; Couque N; Denjoy I; Matrot B; Delclaux C
    J Hypertens; 2023 Aug; 41(8):1339-1346. PubMed ID: 37260279
    [TBL] [Abstract][Full Text] [Related]  

  • 20. PHOX2B mutation-confirmed congenital central hypoventilation syndrome in a Chinese family: presentation from newborn to adulthood.
    Lee P; Su YN; Yu CJ; Yang PC; Wu HD
    Chest; 2009 Feb; 135(2):537-544. PubMed ID: 19201717
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.