Works matching AU Sharma, Suvasini


Results: 185
    1
    2
    3
    4
    5
    6
    7
    8

    Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes.

    Published in:
    Movement Disorders, 2015, v. 30, n. 7, p. 996, doi. 10.1002/mds.26202
    By:
    • Quadri, Marialuisa;
    • Kamate, Mahesh;
    • Sharma, Suvasini;
    • Olgiati, Simone;
    • Graafland, Josja;
    • Breedveld, Guido J.;
    • Kori, Indu;
    • Hattiholi, Virupaxi;
    • Jain, Puneet;
    • Aneja, Satinder;
    • Kumar, Atin;
    • Gulati, Parveen;
    • Goel, Medha;
    • Talukdar, Bibek;
    • Bonifati, Vincenzo
    Publication type:
    Article
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26

    Correspondence.

    Published in:
    2019
    By:
    • Dayal, Devi;
    • Yadav, Jaivinder;
    • Kumar, Prawin;
    • Goyal, Jagdish P.;
    • Vasudevan, Jaishree;
    • Verma, Anjali;
    • Kaushik, Jaya Shankar;
    • Vashishtha, Vipin M.;
    • Pemde, Harish K.;
    • Balasubramanian, S.;
    • Goyal, Alpesh;
    • Rameshkumar, Ramachandran;
    • Kurup, Praveen M.;
    • Paul, Yash;
    • Adhisivam, B.;
    • Sindhu, S.;
    • Virmani, Anju;
    • Sharma, Suvasini;
    • Gupta, Saniya
    Publication type:
    Letter
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36

    Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 5, p. 542, doi. 10.1111/cge.14037
    By:
    • Kaur, Parneet;
    • do Rosario, Michelle C;
    • Hebbar, Malavika;
    • Sharma, Suvasini;
    • Kausthubham, Neethukrishna;
    • Nair, Karthik;
    • A, Shrikiran;
    • Bhat Y, Ramesh;
    • Lewis, Leslie Edward S;
    • Nampoothiri, Sheela;
    • Patil, Siddaramappa J;
    • Suresh, Narayanaswami;
    • Bijarnia Mahay, Sunita;
    • Dua Puri, Ratna;
    • Pai, Shivanand;
    • Kaur, Anupriya;
    • KC, Rakshith;
    • Kamath, Nutan;
    • Bajaj, Shruti;
    • Kumble, Ali
    Publication type:
    Article
    37
    38

    Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population.

    Published in:
    American Journal of Medical Genetics. Part A, 2025, v. 197, n. 3, p. 1, doi. 10.1002/ajmg.a.63914
    By:
    • Kaur, Namanpreet;
    • do Rosario, Michelle C.;
    • Majethia, Purvi;
    • Mascarenhas, Selinda;
    • Rao, Lakshmi Priya;
    • Nair, Karthik Vijay;
    • Hunakunti, Bhagesh;
    • Prasannakumar, Adarsh Pooradan;
    • Naik, Rohit;
    • Narayanan, Dhanya Lakshmi;
    • Nayak, Shalini S.;
    • Bhat, Vivekananda;
    • Sharma, Suvasini;
    • Ramesh Bhat, Y.;
    • Yatheesha, B. L.;
    • Kulkarni, Rajesh;
    • Patil, Siddaramappa J.;
    • Nampoothiri, Sheela;
    • Siddiqui, Shahyan;
    • Girisha, Katta Mohan
    Publication type:
    Article
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49
    50