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2. Hypodipsia-hypernatremia syndrome associated with holoprosencephaly in a child: a case report. Karabay-Bayazit A; Hergüner O; Altunbaşak S; Noyan A; Yükel B; Anarat A Turk J Pediatr; 2002; 44(3):263-6. PubMed ID: 12405444 [TBL] [Abstract][Full Text] [Related]
3. Holoprosencephaly with neurogenic hypernatremia: a new case. Savasta S; Chiapedi S; Borali E; Perrini S; Sepe V; Caimmi S; Marseglia GL Childs Nerv Syst; 2008 Jan; 24(1):139-42. PubMed ID: 17680252 [TBL] [Abstract][Full Text] [Related]
4. Holoprosencephaly and diabetes insipidus in a 3-month-old infant. Kourti M; Pavlou E; Rousso I; Economou I; Athanassiadou F J Child Neurol; 2008 Jan; 23(1):118-20. PubMed ID: 18079312 [TBL] [Abstract][Full Text] [Related]
5. Holoprosencephaly: a case presenting with adipsic hypernatremia. Wang SM; Chen YJ Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1996; 37(3):215-7. PubMed ID: 8755179 [TBL] [Abstract][Full Text] [Related]
6. Hypernatremia after cleft lip repair in a patient with holoprosencephaly. Tung A; Anderson J; Daves S; Waggoner D; Kahana M Anesth Analg; 2006 Mar; 102(3):965-6. PubMed ID: 16492862 [No Abstract] [Full Text] [Related]
7. Profound hypernatremia due to central diabetes insipidus. Vaqar A; Rafiq A; Javaid KH; Parveen R; Sadaf R J Coll Physicians Surg Pak; 2012 Jun; 22(6):409-11. PubMed ID: 22630107 [TBL] [Abstract][Full Text] [Related]
8. [Chronic neurogenic hypernatremia with arhinencephaly]. Perelman R; Czernichow P; Danis F; Nathanson M; Gaudelus J; Cheritat M Ann Pediatr (Paris); 1979 Mar; 26(3):173-8. PubMed ID: 16108279 [No Abstract] [Full Text] [Related]
9. [Chronic neurogenic hypernatremia with arhinencephaly (author's transl)]. Perelman R; Czernichow P; Danis F; Nathanson M; Gaudelus J; Cheritat M Sem Hop; 1979 Nov 8-15; 55(37-38):1727-32. PubMed ID: 230592 [TBL] [Abstract][Full Text] [Related]
10. Organic osmolytes in the brain of an infant with hypernatremia. Schulman M N Engl J Med; 1994 Dec; 331(26):1776-7. PubMed ID: 7984208 [No Abstract] [Full Text] [Related]
11. Severe hypernatremia in an extremely low birth weight infant with subsequent normal neurological development. Sabir H; Stannigel H; Mayatepek E; Hoehn T Neonatology; 2010; 97(2):90-2. PubMed ID: 19707024 [TBL] [Abstract][Full Text] [Related]
12. Lobar holoprosencephaly in a Miniature Schnauzer with hypodipsic hypernatremia. Sullivan SA; Harmon BG; Purinton PT; Greene CE; Glerum LE J Am Vet Med Assoc; 2003 Dec; 223(12):1783-7, 1778. PubMed ID: 14690207 [TBL] [Abstract][Full Text] [Related]
13. The roles of electroencephalography and neuroimaging in children with holoprosencephaly. Yang MT; Lee WT; Peng SS; Lin HC; Tseng CL; Liang JS; Wang PJ; Shen YZ Epileptic Disord; 2004 Sep; 6(3):173-80. PubMed ID: 15504716 [TBL] [Abstract][Full Text] [Related]
14. Clinical features and outcomes of holoprosencephaly in Korea. Ko JM; Kim SH Pediatr Neurol; 2010 Oct; 43(4):245-52. PubMed ID: 20837302 [TBL] [Abstract][Full Text] [Related]
15. Holoprosencephaly presenting as membranous aplasia cutis and diabetes insipidus: report of one case. Tiang MM; Lau BH; Lee TX; Ling MI Acta Paediatr Taiwan; 2004; 45(3):181-3. PubMed ID: 15493741 [TBL] [Abstract][Full Text] [Related]
16. [Semilobar holoprosencephaly associated with central diabetes insipidus]. Arranz Gómez J; Vidal Sampedro J; Herranz Fernández JL; Arteaga Manjón-Cabeza R; Lozano de la Torre MJ An Esp Pediatr; 1987 Nov; 27(5):385-9. PubMed ID: 3326444 [TBL] [Abstract][Full Text] [Related]
17. [Neurogenic hypernatremia. A case observed during the course of a pinealoma]. Schrub JC; Dubuisson M; Hillemand B; Leroy JC Sem Hop; 1970 Jun; 46(30):2084-9. PubMed ID: 4316923 [No Abstract] [Full Text] [Related]
18. [Microcephaly, bilateral corneal opacity and congenital lobar holoprosencephaly with subsequent development of a rhabdomyosarcoma in a patient exposed to prenatal radiation]. García Calatayud S; Arteaga R; Herranz JL Rev Neurol; 2001 Nov 16-30; 33(10):948-51. PubMed ID: 11785006 [TBL] [Abstract][Full Text] [Related]
19. Nasal fistula, epidermal cyst and hypernatremia in a girl presenting holoprosencephaly due to a rare ZIC2 point mutation. de Almeida IG; Kuratani DK; Gomes LM; Fiegenbaum M; Estima Correia EP; Gazzola Zen PR; Machado Rosa RF Eur J Med Genet; 2020 Feb; 63(2):103641. PubMed ID: 30894326 [TBL] [Abstract][Full Text] [Related]