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	121.	WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures. [electronic resource] by Yu, Guang Yu, Man-li Wang, Jia-feng Gao, Cong-rong Chen, Zhong-jin Producer: 20110308 In: Endocrine vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD). [electronic resource] by Pilz, D Quarrell, O W Jones, E W Producer: 19940929 In: Journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Premature coronary artery disease in a patient with Wolfram syndrome. [electronic resource] by Ozer, Necla Okutucu, Sercan Gürses, Kadri Murat Producer: 20120124 In: Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	Longitudinal hearing loss in Wolfram syndrome. [electronic resource] by Karzon, Roanne Narayanan, Anagha Chen, Ling Lieu, Judith E C Hershey, Tamara Producer: 20190415 In: Orphanet journal of rare diseases vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Psychiatric disorders in Wolfram syndrome heterozygotes. [electronic resource] by Owen, M J Producer: 19980427 In: Molecular psychiatry vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Homozygosity for a 4-bp deletion in a patient with Wolfram syndrome suggesting possible phenotype and genotype correlation. [electronic resource] by Sam, W Qin, H Crawford, B Yue, D Yu, S Producer: 20010621 In: Clinical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	Wolframin mutations and hospitalization for psychiatric illness. [electronic resource] by Swift, M Swift, R G Producer: 20051027 In: Molecular psychiatry vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	128.	Observation concerning the age of onset and the nature of optic atrophy in Wolfram's syndrome (DIDMOADS). [electronic resource] by Mayer, U M Rott, H D Böhles, H J Producer: 19851226 In: Ophthalmic paediatrics and genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Wolfram syndrome in a family with variable expression. [electronic resource] by Kadayifci, A Kepekci, Y Coskun, Y Huang, Y Producer: 20020214 In: Acta medica (Hradec Kralove) vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	130.	[Wolfram syndrome]. [electronic resource] by Imataka, George Yamanouchi, Hideo Producer: 20020716 In: Nihon rinsho. Japanese journal of clinical medicine vol. 60 Suppl 4 Availability: No items available. Save to lists Add to cart (remove)
	131.	The relationship between diabetes mellitus and optic atrophy in children. [electronic resource] by Tatham, A Producer: 20091008 In: Diabetic medicine : a journal of the British Diabetic Association vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility. [electronic resource] by Haghighi, Amirreza Haghighi, Alireza Setoodeh, Aria Saleh-Gohari, Nasrollah Astuti, Dewi Barrett, Timothy G Producer: 20130920 In: European journal of human genetics : EJHG vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	[Wolfram syndrome. Three case reports]. [electronic resource] by Hajji, Z Halhal, M Chaoui, Z Chefchaouni, M Agnaou, L Berraho, A Producer: 19990311 In: Journal francais d'ophtalmologie vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	134.	c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. [electronic resource] by Safarpour Lima, Behnam Ghaedi, Hamid Daftarian, Narsis Ahmadieh, Hamid Jamshidi, Javad Khorrami, Mehdi Noroozi, Rezvan Sohrabifar, Nasim Assarzadegan, Farhad Hesami, Omid Taghavi, Shaghayegh Ahmadifard, Azadeh Atakhorrami, Minoo Rahimi-Aliabadi, Simin Shahmohammadibeni, Neda Alehabib, Elham Andarva, Monavvar Darvish, Hossein Emamalizadeh, Babak Producer: 20161006 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4. [electronic resource] by Polymeropoulos, M H Swift, R G Swift, M Producer: 19950106 In: Nature genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	[Genetic diagnosis of diabetes mellitus: Wolfram syndrome--from positional cloning to DNA diagnosis]. [electronic resource] by Tanizawa, Yukio Producer: 20031014 In: Rinsho byori. The Japanese journal of clinical pathology vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	137.	Pigmentary maculopathy in a patient with Wolfram syndrome. [electronic resource] by Dhalla, Mandeep S Desai, Uday R Zuckerbrod, Daniel S Producer: 20070322 In: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	138.	Wolfram syndrome iPS cells: the first human cell model of endoplasmic reticulum disease. [electronic resource] by Urano, Fumihiko Producer: 20140424 In: Diabetes vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	A novel compound heterozygous mutation in an adolescent with insulin-dependent diabetes: The challenge of characterizing Wolfram syndrome. [electronic resource] by Maltoni, Giulio Minardi, Raffaella Cristalli, Carlotta Pia Nardi, Laura D'Alberton, Franco Mantovani, Vilma Zucchini, Stefano Producer: 20170124 In: Diabetes research and clinical practice vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	Complete Wolfram's syndrome and successful pregnancy. [electronic resource] by Rugolo, Salvatore Mirabella, Daniela Palumbo, Marco A Chiantello, Rosalba Fiore, Gaetano Producer: 20030506 In: European journal of obstetrics, gynecology, and reproductive biology vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 454 results.