4 results  1 of 1 

1 Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous COL4A4 Mutation
So Jeong Kim, Jeong Eun Lee, Hyun Duck Kwak, Mi Seon Kang, Seong Ah Yu, Go Hun Seo, Seung Hwan Oh, Woo Yeong Chung
Child Kidney Dis.2021;25(2):128-132.   Published online 2021 December 31     DOI: http://dx.doi.org/10.3339/jkspn.2021.25.2.128
      
2 The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria
Soofia Khan, Michael Schilsky, Gary Silber, Bruce Morgenstern, Tamir Miloh
Pediatr Gastroenterol Hepatol Nutr.2016;19(2):139-142.   Published online 2016 June 28     DOI: http://dx.doi.org/10.5223/pghn.2016.19.2.139
      
3 Anterior Lens Capsule Abnormalities in Alport Syndrome
Jae hyuk Choi, Kyung sool Na, Seon hee Bae, Gyoung hwan Roh
Korean J Ophthalmol.2005;19(1):84-89.   Published online 2005 March 31     DOI: http://dx.doi.org/10.3341/kjo.2005.19.1.84
      
4 Diffuse Esophageal Leiomyomatosis in a Child with Alport Syndrome: Case Report
Hong Seok Ko, Hyun Woo Goo, Chong Hyun Yoon
J Korean Radiol Soc.2004;50(5):375-378.   Published online 2004 May 31     DOI: http://dx.doi.org/10.3348/jkrs.2004.50.5.375
      

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