Author/Creator: Cleary, Maureen A. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Cleary, Maureen A.

1. A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations. Issue 9 (5th August 2013)

Authors:: Shahni, Rojeen; Wedatilake, Yehani; Cleary, Maureen A.; Lindley, Keith J.; Sibson, Keith R.; Rahman, Shamima
Journal:: American journal of medical genetics
Issue:: Volume 161:Issue 9(2013:Sep.)
Page Start:: 2334
Record Type:: Journal Article
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2. A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations. Issue 9 (5th August 2013)

Authors:: Shahni, Rojeen; Wedatilake, Yehani; Cleary, Maureen A.; Lindley, Keith J.; Sibson, Keith R.; Rahman, Shamima
Journal:: American journal of medical genetics
Issue:: Volume 161:Issue 9(2013:Sep.)
Page Start:: 2334
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency. Issue 2 (30th December 2021)

Authors:: Keshavan, Nandaki; Wood, Michelle; Alderson, Lucy M.; Cortina‐Borja, Mario; Skeath, Rachel; McSweeney, Mel; Dixon, Marjorie; Cleary, Maureen A.; Footitt, Emma; Batzios, Spyros
Journal:: JIMD reports
Issue:: Volume 63:Issue 2(2022)
Page Start:: 123
Record Type:: Journal Article
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4. International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome. (23rd October 2018)

Authors:: Parini, Rossella; Broomfield, Alexander; Cleary, Maureen A.; De Meirleir, Linda; Di Rocco, Maja; Fathalla, Waseem M.; Guffon, Nathalie; Lampe, Christina; Lund, Allan M.; Scarpa, Maurizio; Tylki‐Szymańska, Anna; Zeman, Jiří
Journal:: Acta pædiatrica
Issue:: Volume 107:Number 12(2018)
Page Start:: 2059
Record Type:: Journal Article
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