Mandakini Pradhan

Summary

Affiliation: Sanjay Gandhi Postgraduate Institute of Medical Sciences
Country: India

Publications

  1. ncbi request reprint Celiac disease as a rare cause of primary amenorrhea: a case report
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Rae Bareli Road, Lucknow, U P, India
    J Reprod Med 52:453-5. 2007
  2. ncbi request reprint Fertility in men with Down syndrome: a case report
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
    Fertil Steril 86:1765.e1-3. 2006
  3. ncbi request reprint Fetal left ventricular diverticulum presenting as dysrhythmia: diagnosis and management
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    Fetal Diagn Ther 23:10-4. 2008
  4. ncbi request reprint Amiodarone in treatment of fetal supraventricular tachycardia. A case report and review of literature
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, U P, India
    Fetal Diagn Ther 21:72-6. 2006
  5. ncbi request reprint Y chromosome micro-deletions in idiopathic infertility from Northern India
    Rama Devi Mittal
    Department of Urology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India
    Ann Genet 47:331-7. 2004
  6. ncbi request reprint A novel Indian beta-thalassemia mutation in the CACCC box of the promoter region
    Sarita Agarwal
    Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    Eur J Haematol 77:530-2. 2006
  7. ncbi request reprint Genotyping of alpha-thalassemia in microcytic hypochromic anemia patients from North India
    Vaikam H Sankar
    Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    J Appl Genet 47:391-5. 2006
  8. ncbi request reprint MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect
    Ashwin Dalal
    Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
    Gynecol Obstet Invest 63:146-50. 2007
  9. ncbi request reprint Short humerus: an additional antenatal sonographic feature of OFDS type II
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Rae Bareli Road, Lucknow, UP, India 226014, USA
    J Clin Ultrasound 35:390-4. 2007
  10. ncbi request reprint Intrafamilial variability in Fraser syndrome
    Pankaj Prasun
    Sanjay Gandhi Postgraduate Institute of Medical Sciences, Medical Genetics, India
    Prenat Diagn 27:778-82. 2007

Collaborators

Detail Information

Publications13

  1. ncbi request reprint Celiac disease as a rare cause of primary amenorrhea: a case report
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Rae Bareli Road, Lucknow, U P, India
    J Reprod Med 52:453-5. 2007
    ..Primary amenorrhea can be due to abnormal functioning of the hypothalamic-pituitary axis or malformation of müllerian structures. Malnutrition due to chronic malabsorption can alter the axis and can be a cause of primary amenorrhea...
  2. ncbi request reprint Fertility in men with Down syndrome: a case report
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
    Fertil Steril 86:1765.e1-3. 2006
    ..To inform clinicians about fertility in males with Down syndrome...
  3. ncbi request reprint Fetal left ventricular diverticulum presenting as dysrhythmia: diagnosis and management
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    Fetal Diagn Ther 23:10-4. 2008
    ..Restoration of fetal sinus rhythm was achieved within 48 h. Serial fetal echocardiograms were performed every week, followed by a normal vaginal delivery at term. The child is surviving at 1 year of age...
  4. ncbi request reprint Amiodarone in treatment of fetal supraventricular tachycardia. A case report and review of literature
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, U P, India
    Fetal Diagn Ther 21:72-6. 2006
    ..Conversion to sinus rhythm and resolution of hydrops followed this treatment. Since there is no ideal treatment protocol for these cases at present, we reviewed reports of transplacental treatment of SVT...
  5. ncbi request reprint Y chromosome micro-deletions in idiopathic infertility from Northern India
    Rama Devi Mittal
    Department of Urology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India
    Ann Genet 47:331-7. 2004
    ..Deletions were detected with known and unknown aetiology and at least in one of the infertile male with varicocele. AZF micro-deletions seen in idiopathic infertile males suggest the need for molecular screening in non-idiopathic cases...
  6. ncbi request reprint A novel Indian beta-thalassemia mutation in the CACCC box of the promoter region
    Sarita Agarwal
    Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    Eur J Haematol 77:530-2. 2006
    ..This is the first report of a previously undescribed mutation in Indian subjects of the CACCC box of promoter region for beta-globin, which in combination with a common mutation produces thalassemia major in the offspring of the family...
  7. ncbi request reprint Genotyping of alpha-thalassemia in microcytic hypochromic anemia patients from North India
    Vaikam H Sankar
    Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India
    J Appl Genet 47:391-5. 2006
    ..The a-gene mutation is quite common in the Indian subcontinent. Molecular genotyping of a-thalassemia helps to diagnose unexplained microcytosis, and thus prevents unnecessary iron supplementation...
  8. ncbi request reprint MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect
    Ashwin Dalal
    Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
    Gynecol Obstet Invest 63:146-50. 2007
    ..Since the closure of neural tube occurs at multiple sites, the etiology of defect at different sites may be different - which explains the failure of folic acid supplementation to prevent all NTDs...
  9. ncbi request reprint Short humerus: an additional antenatal sonographic feature of OFDS type II
    Mandakini Pradhan
    Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Rae Bareli Road, Lucknow, UP, India 226014, USA
    J Clin Ultrasound 35:390-4. 2007
    ..We report a case of oral-facial-digital syndrome type II that presented antenatally with polyhydramnios, short humerus, polydactyly, and duplicated thumb...
  10. ncbi request reprint Intrafamilial variability in Fraser syndrome
    Pankaj Prasun
    Sanjay Gandhi Postgraduate Institute of Medical Sciences, Medical Genetics, India
    Prenat Diagn 27:778-82. 2007
    ..It has not been reported before and highlights the importance of careful screening of pregnancies in families with Fraser syndrome...
  11. ncbi request reprint Limb body wall complex
    Pankaj Prasun
    Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow 226 014, UP, India
    Indian J Pathol Microbiol 51:255-6. 2008
    ..The authors report a case of LBWC diagnosed in early antenatal period. The pregnancy was terminated following the diagnosis. Fetal autopsy findings were typical of LBWC...
  12. ncbi request reprint Molecular characterization of thalassemia intermedia in Indians
    Inusha Panigrahi
    Haematologica 91:1279-80. 2006
    ..In heterozygous beta-thalassemia, alphaalphaalphaanti-3.7 triplication was the predominant factor (14/23 cases)...
  13. ncbi request reprint Shortcomings of the Prenatal Diagnostic Techniques Act, 1994
    Mandakini Pradhan
    Natl Med J India 17:342. 2004