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Publications by M E Carruthers

Hereditary Crystalline Stromal Dystrophy of Schnyder. I. Clinical Features of a Family With Hyperlipoproteinaemia.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1972English

Flexible Electrophoresis Applicator for Use With the AutoAnalyzer in Routine Protein Analysis.

Journal of Clinical Pathology
MedicineForensic MedicinePathology
1970English

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Clinical and Genetic Features in Italian Bietti Crystalline Dystrophy Patients

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2012English

Clinical Features of a Pediatric Case With Cone Dystrophy

Van Medical Journal
2018English

Clinical Diversity in Patients With Schnyder Corneal Dystrophy—a Novel and Known UBIAD1 Pathogenic Variants

Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2018English

Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy

PLoS ONE
Multidisciplinary
2007English

Mutations in theUBIAD1Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2007English

Hereditary Retinal Dystrophy

2020English

Probable Common Origin of a Hereditary Fundus Dystrophy (Sorsby's Familial Pseunflammatory Macular Dystrophy) in an English and Australian Family.

Journal of Medical Genetics
Genetics
1976English

Bietti Crystalline Dystrophy

2020English

Pancreatitis Induced by Oestrogen in a Patient With Type I Hyperlipoproteinaemia.

BMJ
1986English

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