Search Results - "Huq, A.H.M. M."

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  1. 1

    Infantile Spasms Are Associated With Abnormal Copy Number Variations by Tiwari, Vijay N., Sundaram, Senthil K., Chugani, Harry T., Huq, A.H.M. M.

    Published in Journal of child neurology (01-10-2013)
    “…The authors tested the hypothesis that de novo copy number variations (CNVs) implicated in known genomic disorders (“pathogenic CNVs”) are significant…”
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  2. 2

    Advances in Tourette Syndrome by Serajee, Fatema J., MD, Mahbubul Huq, A.H.M., MD, PhD

    Published in The Pediatric clinics of North America (01-06-2015)
    “…Tourette syndrome (TS) is a childhood-onset neurodevelopmental disorder characterized by multiple motor tics and at least one vocal or phonic tic, and often…”
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  3. 3

    Abnormal Language Pathway in Children With Angelman Syndrome by Wilson, Benjamin J., BA, Sundaram, Senthil K., MD, Huq, A.H.M., MD, PhD, Jeong, Jeong-Won, PhD, Halverson, Stacey R., MS, Behen, Michael E., PhD, Bui, Duy Q., BS, Chugani, Harry T., MD

    Published in Pediatric neurology (01-05-2011)
    “…Angelman syndrome is a genetic disorder characterized by pervasive developmental disability with failure to develop speech. We examined the basis for severe…”
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  4. 4

    Evaluation of Neuroinflammation in X-Linked Adrenoleukodystrophy by Kumar, Ajay, MD, PhD, DNB, Chugani, Harry T., MD, Chakraborty, Pulak, PhD, Huq, A.H.M. Mahbubul, MD, PhD

    Published in Pediatric neurology (01-02-2011)
    “…We present findings of11 C-[R]-PK11195 positron emission tomography in a child with X-linked adrenoleukodystrophy.11 C-[R]-PK11195 is a radioligand with a high…”
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  5. 5

    Peripheral blood stem cell autotransplantation in treatment of childhood cancer by Watanabe, T, Takaue, Y, Kawano, Y, Koyama, T, Huq, M A, Shimokawa, T, Ninomiya, T, Aga, Y, Inai, T, Hino, M

    Published in Bone marrow transplantation (Basingstoke) (01-05-1989)
    “…The levels of circulating hematopoietic progenitor cells were measured sequentially in eight children receiving chemotherapy for acute leukemia or…”
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