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 *

229 related articles for article (PubMed ID: 23498571)

  • 1. Oral-facial-digital syndrome type 1 with hypothalamic hamartoma and Dandy-Walker malformation.
    Azukizawa T; Yamamoto M; Narumiya S; Takano T
    Pediatr Neurol; 2013 Apr; 48(4):329-32. PubMed ID: 23498571
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypothalamic hamartoma in oral-facial-digital syndrome type VI (Váradi syndrome).
    Stephan MJ; Brooks KL; Moore DC; Coll EJ; Goho C
    Am J Med Genet; 1994 Jun; 51(2):131-6. PubMed ID: 8092188
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oral-facial-digital syndrome with hypothalamic hamartoma, postaxial ray hypoplasia of the limbs, and vagino-cystic communication: a new variant?
    Fujiwara I; Kondo Y; Iinuma K
    Am J Med Genet; 1999 Mar; 83(2):77-81. PubMed ID: 10190476
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Agenesis of the corpus callosum and Dandy-Walker malformation associated with hemimegalencephaly in the sebaceous nevus syndrome.
    Dodge NN; Dobyns WB
    Am J Med Genet; 1995 Mar; 56(2):147-50. PubMed ID: 7625436
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oral-facial-digital syndrome type IX in a patient with Dandy-Walker malformation.
    Nagai K; Nagao M; Nagao M; Yanai S; Minagawa K; Takahashi Y; Takekoshi Y; Ishizaka A; Matsuzono Y; Kobayashi O; Itagaki T
    J Med Genet; 1998 Apr; 35(4):342-4. PubMed ID: 9598735
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Oral-facial-digital syndrome type I in a newborn male.
    Gillerot Y; Heimann M; Fourneau C; Verellen-Dumoulin C; Van Maldergem L
    Am J Med Genet; 1993 May; 46(3):335-8. PubMed ID: 8488880
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dandy-Walker malformation: a rare association with hypoparathyroidism.
    Coban D; Akin MA; Kurtoglu S; Oktem S; Yikilmaz A
    Pediatr Neurol; 2010 Dec; 43(6):439-41. PubMed ID: 21093738
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Mohr syndrome: are there two variants?
    Haumont D; Pelc S
    Clin Genet; 1983 Jul; 24(1):41-6. PubMed ID: 6352094
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coexistance of cerebral sinovenous thrombosis and Dandy Walker malformation in newborn.
    Gverić-Ahmetasević S; Colić A; Gverić T; Gasparović VE; Pavlisa G; Ozretić D
    Coll Antropol; 2011 Jan; 35 Suppl 1():303-7. PubMed ID: 21648352
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gelastic epilepsy, hypothalamic hamartoma, precocious puberty, and agenesis of the corpus callosum: a new association.
    Alikchanov AA; Petrukhin AS; Mukhin KYu ; Nikanorov AYu
    Brain Dev; 1998 Jun; 20(4):239-41. PubMed ID: 9661969
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rhombencephalosynapsis associated with Dandy-Walker malformation.
    Sener RN
    J Neuroimaging; 2007 Oct; 17(4):355-7. PubMed ID: 17894629
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dandy-Walker syndrome together with occipital encephalocele.
    Cakmak A; Zeyrek D; Cekin A; Karazeybek H
    Minerva Pediatr; 2008 Aug; 60(4):465-8. PubMed ID: 18511899
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Differential diagnosis of syndromes with abnormal respiration (tachypnea-apnea).
    Boltshauser E; Lange B; Dumermuth G
    Brain Dev; 1987; 9(5):462-5. PubMed ID: 3434721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ORAL-FACIAL-DIGITAL SYNDROME TYPE I (CLINICAL CASE).
    Horlenko O; Lenchenko A; Kossey G; Tomey A; Debretseni O
    Georgian Med News; 2018 Dec; (285):47-51. PubMed ID: 30702069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rubinstein-Taybi syndrome associated with Dandy-Walker cyst. Case report in a newborn.
    Mazzone D; Milana A; Praticò G; Reitano G
    J Perinat Med; 1989; 17(5):381-4. PubMed ID: 2625658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs.
    Haug K; Khan S; Fuchs S; König R
    Am J Med Genet; 2000 Mar; 91(2):135-7. PubMed ID: 10748413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. C5orf42 is the major gene responsible for OFD syndrome type VI.
    Lopez E; Thauvin-Robinet C; Reversade B; Khartoufi NE; Devisme L; Holder M; Ansart-Franquet H; Avila M; Lacombe D; Kleinfinger P; Kaori I; Takanashi J; Le Merrer M; Martinovic J; Noël C; Shboul M; Ho L; Güven Y; Razavi F; Burglen L; Gigot N; Darmency-Stamboul V; Thevenon J; Aral B; Kayserili H; Huet F; Lyonnet S; Le Caignec C; Franco B; Rivière JB; Faivre L; Attié-Bitach T
    Hum Genet; 2014 Mar; 133(3):367-77. PubMed ID: 24178751
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.
    Ben Hamouda H; Sfar MN; Braham R; Ben Salah M; Ayadi A; Soua H; Hamza H; Sfar MT
    Acta Orthop Belg; 2001 Dec; 67(5):528-32. PubMed ID: 11822087
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuropathology of oral-facial-digital syndromes.
    Towfighi J; Berlin CM; Ladda RL; Frauenhoffer EE; Lehman RA
    Arch Pathol Lab Med; 1985 Jul; 109(7):642-6. PubMed ID: 3839363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Aicardi syndrome with Dandy-Walker type malformation].
    Laguado-Herrera YV; Manrique-Hernández EF; Peñaloza-Mantilla CA; Quintero-Gómez DA; Contreras-García GA; Sandoval-Martínez DK
    Rev Neurol; 2015 Jul; 61(2):71-4. PubMed ID: 26156442
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.