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  Access statistics : Table of Contents
   2018| January-March  | Volume 19 | Issue 1  
    Online since December 28, 2017

 
 
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REVIEW ARTICLE
Stevens-Johnson syndrome and toxic epidermal necrolysis in children
Sudip Das, Ramkumar Ramamoorthy
January-March 2018, 19(1):9-14
DOI:10.4103/ijpd.IJPD_120_17  
  8,332 1,084 1
CASE REPORTS
Tinea capitis in children: A report of four cases trichoscopic with trichoscopic features
Ebtisam Elghblawi
January-March 2018, 19(1):51-56
DOI:10.4103/ijpd.IJPD_145_16  
  3,459 338 1
CME ARTICLE
Vascular birthmarks: A hidden world behind a word
Carlo Gelmetti
January-March 2018, 19(1):1-8
DOI:10.4103/ijpd.IJPD_124_17  
  2,233 455 -
ORIGINAL ARTICLES
Unusual presentations and associations of hyper IgE Syndrome: Retrospective analysis of ten cases at tertiary care institute – With review of indian published reports
Nayan H Patel, Jigna K Padhiyar, Yogesh B Shah, Trusha P Gajjar, Mansi D Buch
January-March 2018, 19(1):31-36
DOI:10.4103/ijpd.IJPD_144_16  
  2,385 284 -
Childhood leprosy in the postelimination era: A vision achieved or a concern growing at large
Ashwini Babu, M Ramesh Bhat, Jyothi Jayaraman
January-March 2018, 19(1):26-30
DOI:10.4103/ijpd.IJPD_132_16  
  2,193 317 4
LETTERS TO EDITOR
Legius syndrome
Manoj Kumar Sharma, Ramesh Kumar, Savera Gupta, Suresh Kumar Jain
January-March 2018, 19(1):86-88
DOI:10.4103/ijpd.IJPD_143_16  
  2,198 193 -
ORIGINAL ARTICLES
Study of physiological and pathological skin changes in neonates: An east indian perspective
Binodini Behera, Yatra Kavadya, Prasenjit Mohanty, Dipanweeta Routray, Subhra Ghosh, Lina Das
January-March 2018, 19(1):40-47
DOI:10.4103/ijpd.IJPD_21_17  
  2,038 273 1
Effect of occurrence of vitiligo in children over quality of life of their families: A hospital-based study using family dermatology life quality index
Pratik Gahalaut, Sandhya Chauhan, Amit Shekhar, Madhur Kant Rastogi, Nitin Mishra
January-March 2018, 19(1):21-25
DOI:10.4103/ijpd.IJPD_136_16  
  1,976 265 -
CASE REPORTS
Congenital insensitivity to pain: Case report of a rare entity
Swati Dahiya, Kondajji Ramchandra Vijayalakshmi, Mubeen Khan
January-March 2018, 19(1):48-50
DOI:10.4103/ijpd.IJPD_142_16  
  1,921 185 -
LETTERS TO EDITOR
Hoyeraal–Hreidarsson syndrome: A rare dyskeratosis congenita phenotype
Mansoor C Abdulla
January-March 2018, 19(1):83-84
DOI:10.4103/ijpd.IJPD_140_16  
  1,631 155 -
ORIGINAL ARTICLES
Cutaneous leishmaniasis in children: A case series
Mrinal Gupta
January-March 2018, 19(1):37-39
DOI:10.4103/ijpd.IJPD_148_16  
  1,527 227 -
Prevalence of dermatoses among the tribal children studying in residential schools of South Chhattisgarh, India
Yasha Upendra, Sampreeti Sendur, Naveen Keswani, Abhishek Pallava
January-March 2018, 19(1):15-20
DOI:10.4103/ijpd.IJPD_128_16  
  1,474 250 -
CASE REPORTS
Recurrent pilomatricoma of the thigh: An unusual site of presentation
Vanlalhriatpuii Hmar, Nandakishore Thokchom, Sandhyarani Kshetrimayum
January-March 2018, 19(1):65-67
DOI:10.4103/ijpd.IJPD_72_16  
  1,544 143 -
Dermatopathia pigmentosa reticularis
Gauri Vats, Rohit Kataria, Durgesh Sonare, Vinod Jain
January-March 2018, 19(1):77-79
DOI:10.4103/ijpd.IJPD_79_16  
  1,470 165 2
Ecthyma gangrenosum as the presenting clinical feature of autoimmune lymphoproliferative syndrome
Aniruddha Ghosh, Rashmita Das, Partha Pratim Halder, Sandipan Dhar
January-March 2018, 19(1):62-64
DOI:10.4103/ijpd.IJPD_141_16  
  1,261 154 -
Cutaneous polyarteritis nodosa: Diagnosis lies skin deep
Raghavendraswami Amoghimath, Rajwanti K Vaswani, Chandrahas T Deshmukh, Chhaya Divecha
January-March 2018, 19(1):71-73
DOI:10.4103/ijpd.IJPD_138_16  
  1,206 156 -
Monomorphic bullous hemorrhagic varicella in a patient on methotrexate
Swastika Suvirya, Amita Jain, Avinash Agrawal, Parul Jain
January-March 2018, 19(1):59-61
DOI:10.4103/ijpd.IJPD_6_15  
  1,207 147 1
LETTERS TO EDITOR
Twin-spot phenomenon: A rare association hypomelanosis of ito with nevoid hypertrichosis
Projna Biswas, Abhishek De , Dayamay Pal, Asad Ansari, Sudip Das
January-March 2018, 19(1):88-90
DOI:10.4103/ijpd.IJPD_139_16  
  1,121 145 -
Autosomal recessive anhidrotic ectodermal dysplasia: A rare disease
Tasleem Arif, Mohammad Adil, Syed Suhail Amin, Konchok Dorjay
January-March 2018, 19(1):84-86
DOI:10.4103/ijpd.IJPD_116_16  
  1,066 134 1
CASE REPORTS
A rare case of neurocutaneous disorders of the newborn: Incontinentia pigmenti
Melek Aslan Kayiran, Mehmet Salih Gürel, Burçe Can Kuru, Ilkin Zindancı
January-March 2018, 19(1):68-70
DOI:10.4103/ijpd.IJPD_135_16  
  1,014 154 -
Dego's disease in a female child with Anti-Scl-70 antibody positivity
Jigna Krunal Padhiyar, Nayan H Patel, Trusha P Gajjar, Mansi D Buch
January-March 2018, 19(1):80-82
DOI:10.4103/ijpd.IJPD_84_17  
  929 141 -
Kasabach–Merritt syndrome in an infant successfully treated with a combination of propranolol and methotrexate
Thulasi Weerasinghe, AC Ranasinghe, Jayamini Seneviratne
January-March 2018, 19(1):57-58
DOI:10.4103/ijpd.IJPD_137_16  
  902 164 -
A rare co-existence of langerhans cell histiocytosis and lichen planus
Aarti S Salunke, Anil P Gosavi, Ravindranath B Chavan, Pallavi Prataprao Patil
January-March 2018, 19(1):74-76
DOI:10.4103/ijpd.IJPD_147_16  
  868 129 -
ERRATUM
Erratum: Tinea Capitis in Children: A Report of Four Cases Trichoscopic with Trichoscopic features

January-March 2018, 19(1):91-91
DOI:10.4103/2319-7250.222806  
  340 103 -
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