Search Results - "Waghela, Sneha"

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  1. 1

    Spectrum of afibrinogenemia: Bleeding to thrombosis- retrospective analysis of five patients by Waghela, Sneha, Sharma, Sujata, Shah, Nikita, Uchil, Harshada, Ghildiyal, Radha

    Published in Pediatric hematology oncology journal (01-03-2024)
    “…Afibrinogenemia is a rare disorder, with autosomal recessive inheritance, most often associated with consanguinity. To date, very few cases have been reported…”
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    Journal Article
  2. 2

    Alloimmunization in children with sickle cell disease: A tertiary care experience by Sharma, Sujata, Parikh, Lekha, Shah, Nikita, Waghela, Sneha, Ghildiyal, Radha

    Published in Pediatric hematology oncology journal (01-06-2023)
    “…Patients with sickle cell disease (SCD) show a high prevalence of red blood cell (RBC) alloimmunization, however, few studies have focused on children. The…”
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    Journal Article
  3. 3

    Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin by Waghela, Sneha, Sharma, Sujata, Shah, Nikita, Uchil, Harshada, Ghildiyal, Radha

    Published in Pediatric hematology oncology journal (01-03-2023)
    “…Delta-beta thalassemia and hereditary persistence of fetal hemoglobin (HPFH) results from a deletion in both the delta and beta genes on chromosome 11…”
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    Journal Article
  4. 4

    Clinical profile and predictors for outcome in children presenting with Guillain-Barré syndrome by Singh, Sonali, Gupta, Nitin, Gupta, Arpita, Chandel, Anurag, Waghela, Sneha, Saple, Pallavi

    “…Introduction: Acute Flaccid Paralysis (AFP) is a group of diverse clinical conditions with Guillain-Barré syndrome (GBS) as one of the most common cause. The…”
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    Journal Article
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