Search Results - Jim McGill

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  1. 21
    Fourier Transform Infrared Reflectance Spectra of Latent Fingerprints: A Biometric Gauge for the Age of an Individual

    Fourier Transform Infrared Reflectance Spectra of Latent Fingerprints: A Biometric Gauge for the Age of an Individual by Hemmila, April, McGill, Jim, Ritter, David

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  2. 22
    Successful management of severe coronoid process hyperplasia in a patient with mucopolysaccharidosis VI: a case report

    Successful management of severe coronoid process hyperplasia in a patient with mucopolysaccharidosis VI: a case report by Khadembaschi, Darius, Arvier, John, Beech, Nicholas, Dolan, David, McGill, Jim

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  3. 23
    Depressive symptoms in adolescents with early and continuously treated phenylketonuria: Associations with phenylalanine and tyrosine levels

    Depressive symptoms in adolescents with early and continuously treated phenylketonuria: Associations with phenylalanine and tyrosine levels by Sharman, Rachael, Sullivan, Karen, Young, Ross McD, McGill, Jim

    Published in Gene
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  4. 24
    Deep bed farming and the SMART approach for reaching the SDGs for climate and water

    Deep bed farming and the SMART approach for reaching the SDGs for climate and water by Henk Holtslag, Jim McGill

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  5. 25
    A Preliminary Investigation of the Role of the Phenylalynine:Tyrosine Ratio in Children With Early and Continuously Treated Phenylketonuria: Toward Identification of "Safe" Levels

    A Preliminary Investigation of the Role of the Phenylalynine:Tyrosine Ratio in Children With Early and Continuously Treated Phenylketonuria: Toward Identification of "Safe" Levels by Sharman, Rachael, Sullivan, Karen, Young, Ross, McGill, Jim

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  6. 26
    Executive functioning of 4 children with hyperphenylalaninemia from childhood to adolescence

    Executive functioning of 4 children with hyperphenylalaninemia from childhood to adolescence by Sharman, Rachael, Sullivan, Karen A, Jones, Toni, Young, Ross McD, McGill, Jim

    Published in Pediatrics (Evanston)
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  7. 27
    Nutrition process improvements for adult inpatients with inborn errors of metabolism using the i‐PARIHS framework

    Nutrition process improvements for adult inpatients with inborn errors of metabolism using the i‐PARIHS framework by Williams, Clare, van der Meij, Barbara S., Nisbet, Janelle, Mcgill, Jim, Wilkinson, Shelley A.

    Published in Nutrition & dietetics
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  8. 28
    Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

    Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families by Kamarinos, Maria, McGill, Jim, Lynch, Michael, Dahl, Henrik

    Published in Human mutation
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  9. 29
    Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI)

    Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI) by Choy, Yew Sing, Bhattacharya, Kaustuv, Balasubramaniam, Shanti, Fietz, Michael, Fu, Antony, Inwood, Anita, Jin, Dong-Kyu, Kim, Ok-Hwa, Kosuga, Motomichi, Kwun, Young Hee, Lin, Hsiang-Yu, Lin, Shuan-Pei, Mendelsohn, Nancy J., Okuyama, Torayuki, Samion, Hasri, Tan, Adeline, Tanaka, Akemi, Thamkunanon, Verasak, Thong, Meow-Keong, Toh, Teck-Hock, Yang, Albert D., McGill, Jim

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  10. 30
    Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB

    Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB by Zankl, Andreas, Duncan, Emma L., Leo, Paul J., Clark, Graeme R., Glazov, Evgeny A., Addor, Marie-Claude, Herlin, Troels, Kim, Chong Ae, Leheup, Bruno P., McGill, Jim, McTaggart, Steven, Mittas, Stephen, Mitchell, Anna L., Mortier, Geert R., Robertson, Stephen P., Schroeder, Marie, Terhal, Paulien, Brown, Matthew A.

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  11. 31
    Using the Simulation Center to Perform Yearly Competencies of Environmental Service Workers: A Multi-disciplinary Approach to Training

    Using the Simulation Center to Perform Yearly Competencies of Environmental Service Workers: A Multi-disciplinary Approach to Training by Marek, Maryellen, MLT (ASCP), MS, BSN, RN, CIC, Kutzin, Jared, DNP, MS, MPH, RN, CPPS, Gross, David, BA, EMT, Guzman, Luz, Joseph, Vernon, Yaney, Eileen, MT, MS, CIC, McGill, Jim

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  12. 32
    Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

    Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families by Kamarinos, Maria, McGill, Jim, Lynch, Michael, Dahl, Henrik

    Published in Human mutation
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  13. 33
    Congenital disorder of glycosylation type Ia presenting as early-onset cerebellar ataxia in an adult

    Congenital disorder of glycosylation type Ia presenting as early-onset cerebellar ataxia in an adult by Schoffer, Kerrie L., O'Sullivan, John D., McGill, Jim

    Published in Movement disorders
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  14. 34
    The molecular basis of cystathionine β-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment

    The molecular basis of cystathionine β-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment by Gaustadnes, Mette, Wilcken, Bridget, Oliveriusova, Jana, McGill, Jim, Fletcher, Janice, Kraus, Jan P., Wilcken, David E.

    Published in Human mutation
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  15. 35
    A preliminary investigation of the role of the phenylalanine:tyrosine ratio in children with early and continuously treated phenylketonuria: toward identification of "safe" levels

    A preliminary investigation of the role of the phenylalanine:tyrosine ratio in children with early and continuously treated phenylketonuria: toward identification of "safe" levels by Sharman, Rachael, Sullivan, Karen, Young, Ross, McGill, Jim

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  16. 36
    Erratum: Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

    Erratum: Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families by Kamarinos, Maria, McGill, Jim, Lynch, Michael, Dahl, Henrik

    Published in Human mutation
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  17. 37
    Erratum: Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

    Erratum: Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families by Kamarinos, Maria, McGill, Jim, Lynch, Michael, Dahl, Henrik

    Published in Human mutation
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  18. 38
    Hepatocellular carcinoma requiring liver transplantation in hereditary tyrosinemia type 1 despite nitisinone therapy and α1-fetoprotein normalization

    Hepatocellular carcinoma requiring liver transplantation in hereditary tyrosinemia type 1 despite nitisinone therapy and α1-fetoprotein normalization by Bhushan, Shreya, Noble, Charlton, Balouch, Fariha, Lewindon, Peter, Lampe, Guy, Hodgkinson, Peter, McGill, Jim, Ee, Looi

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  19. 39
    The molecular basis of cystathionine ²-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment

    The molecular basis of cystathionine ²-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment by Gaustadnes, Mette, Wilcken, Bridget, Oliveriusova, Jana, McGill, Jim, Fletcher, Janice, Kraus, Jan P, Wilcken, David E

    Published in Human mutation
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  20. 40
    The molecular basis of cystathionine ?-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment

    The molecular basis of cystathionine ?-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment by Gaustadnes, Mette, Wilcken, Bridget, Oliveriusova, Jana, McGill, Jim, Fletcher, Janice, Kraus, Jan P., Wilcken, David E.

    Published in Human mutation
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