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.
5. Feeding problems and malnutrition in spinal muscular atrophy type II. Messina S; Pane M; De Rose P; Vasta I; Sorleti D; Aloysius A; Sciarra F; Mangiola F; Kinali M; Bertini E; Mercuri E Neuromuscul Disord; 2008 May; 18(5):389-93. PubMed ID: 18420410 [TBL] [Abstract][Full Text] [Related]
6. Arthrogryposis multiplex congenita and pituitary ectopia. A case report. Parano E; Trifiletti RR; Barone R; Pavone V; Pavone P Neuropediatrics; 2000 Dec; 31(6):325-7. PubMed ID: 11508555 [TBL] [Abstract][Full Text] [Related]
9. A proposed multidisciplinary approach for identifying feeding abnormalities in children with cerebral palsy. Santoro A; Lang MB; Moretti E; Sellari-Franceschini S; Orazini L; Cipriani P; Cioni G; Battini R J Child Neurol; 2012 Jun; 27(6):708-12. PubMed ID: 22019841 [TBL] [Abstract][Full Text] [Related]
10. Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects. Hall JG J Pediatr Orthop B; 1997 Jul; 6(3):159-66. PubMed ID: 9260643 [TBL] [Abstract][Full Text] [Related]
11. Identifying feeding and swallowing problems in infants and young children. Imhoff SM; Wigginton VM Clin Commun Disord; 1991; 1(2):59-67. PubMed ID: 1844854 [No Abstract] [Full Text] [Related]
12. Arthrogryposis multiplex congenita and bilateral parietal polymicrogyria in association with the intrauterine death of a twin. Baker EM; Khorasgani MG; Gardner-Medwin D; Gholkar A; Griffiths PD Neuropediatrics; 1996 Feb; 27(1):54-6. PubMed ID: 8677028 [TBL] [Abstract][Full Text] [Related]
13. Arthrogryposis multiplex congenita--a rare congenital anomaly. Suryawanshi C; Panditrao MM; Panditrao MM; Rai I J Indian Med Assoc; 2006 Feb; 104(2):95-6, 98. PubMed ID: 16856591 [TBL] [Abstract][Full Text] [Related]