CT findings in a child with reflux oesophagitis.

Autor: Crankson S; King Abdulaziz Medical City-Riyadh, King Fahad National Guard Hospital P.O. Box 22490, Riyadh 11426, Saudi Arabia. cranksons@yahoo.com, Al Salman MJ, Al Mane KA, Al Zaben AA

Publikováno v: Tropical gastroenterology : official journal of the Digestive Diseases Foundation [Trop Gastroenterol] 2004 Jan-Mar; Vol. 25 (1), pp. 47-8.

Extrinsic duodenal obstruction from anomalous congenital band.

Autor: Crankson SJ; Department of Surgery, King Fahad National Guard Hospital, Riyadh, Saudi Arabia. cranksons@ngha.med.sa, Al-Mane KA, Al-Zaben A, Al-Dhafian A

Publikováno v: Annals of Saudi medicine [Ann Saudi Med] 2000 Sep-Nov; Vol. 20 (5-6), pp. 443-4.

Raine's syndrome: rare disease from neurosurgical perspective.

Autor: Elmaghraby M; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK. mostafa.elmaghraby@azhar.edu.eg.; Neurosurgery Department, Faculty of Medicine, Al-Azhar University, Cairo, Egypt. mostafa.elmaghraby@azhar.edu.eg., Abrar S; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK., Kanangi SMR; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK., Parks C; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK., Duncan C; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK., Richardson D; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK., Sinha A; Neurosurgery Department, Alder Hey Children Hospital, Liverpool, UK.

Publikováno v: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2024 Jan; Vol. 40 (1), pp. 11-17. Date of Electronic Publication: 2023 Oct 11.

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations.

Autor: Acevedo, Ana Carolina¹ acevpoppe@gmail.com, Poulter, James A.² a.j.mighell@leeds.ac.uk, Alves, Priscila Gomes¹, de Lima, Caroline Lourenço¹, Castro, Luiz Claudio³, Yamaguti, Paulo Marcio¹, Paula, Lilian M.¹, Parry, David A.⁴, Logan, Clare V.², Smith, Claire E. L.², Johnson, Colin A.², Inglehearn, Chris F.², Mighell, Alan J.^2,5

Publikováno v: BMC Medical Genetics. 2015, Vol. 16 Issue 1, p1-11. 11p.

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age.

Autor: Eltan, Mehmet, Alavanda, Ceren, Yavas Abali, Zehra, Ergenekon, Pinar, Yalındag Ozturk, Nilufer, Sakar, Mustafa, Dagcinar, Adnan, Kirkgoz, Tarik, Kaygusuz, Sare Betul, Gokdemir, Yasemin, Elcioglu, Huriye Nursel, Guran, Tulay, Bereket, Abdullah, Ata, Pinar, Turan, Serap

Publikováno v: Calcified Tissue International; Jul2020, Vol. 107 Issue 1, p96-103, 8p