Published in Clin Dysmorphol on July 01, 2002
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Brain size regulations by cbp haploinsufficiency evaluated by in-vivo MRI based volumetry. Sci Rep (2015) 0.75
Idiopathic chronic pancreatitis in India: phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations. Gut (2010) 3.63
Light emitting diodes versus compact fluorescent tubes for phototherapy in neonatal jaundice: a multi center randomized controlled trial. Indian Pediatr (2009) 2.47
Evaluation of phototherapy devices used for neonatal hyperbilirubinemia. Indian Pediatr (2010) 2.04
Novel mutations in Indian patients with autosomal recessive infantile malignant osteopetrosis. Indian J Med Res (2010) 1.98
Sequential occurrence of preneoplastic lesions and accumulation of loss of heterozygosity in patients with gallbladder stones suggest causal association with gallbladder cancer. Ann Surg (2014) 1.82
Incidence of acute kidney injury in hospitalized children. Indian Pediatr (2011) 1.80
Efficacy of zinc in reducing hyperbilirubinemia among at-risk neonates: a randomized, double-blind, placebo-controlled trial. Indian J Pediatr (2011) 1.76
Association of SPINK1 gene mutation and CFTR gene polymorphisms in patients with pancreas divisum presenting with idiopathic pancreatitis. J Clin Gastroenterol (2009) 1.65
Intravenous pamidronate therapy in osteogenesis imperfecta: response to treatment and factors influencing outcome. J Pediatr Orthop (2007) 1.58
Sepsis in the newborn. Indian J Pediatr (2008) 1.58
Hypocalcemia in the newborn. Indian J Pediatr (2010) 1.55
Efficacy of oral phenobarbitone in term "at risk" neonates in decreasing neonatal hyperbilirubinemia: a randomized double-blinded, placebo controlled trial. Indian Pediatr (2004) 1.54
Serum leptin levels in obese Indian children relation to clinical and biochemical parameters. Indian Pediatr (2007) 1.51
Effect of sling application on efficacy of phototherapy in healthy term neonates with nonhemolytic jaundice: a randomized conrolled trial. Indian Pediatr (2009) 1.49
Central diabetes insipidus: clinical profile and factors indicating organic etiology in children. Indian Pediatr (2008) 1.48
Unconjugated hyperbilirubinemia in newborns: current perspective. Indian Pediatr (2002) 1.45
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing. Hum Mutat (2007) 1.44
Neonatal hypernatremia due to high breast-milk sodium. Indian Pediatr (2002) 1.44
Alpha 1 antitrypsin deficiency in children with chronic liver disease in North India. Indian Pediatr (2009) 1.44
Early iron supplementation in very low birth weight infants--a randomized controlled trial. Acta Paediatr (2009) 1.43
Brachytelephalangic chondrodysplasia punctata: a case series to further delineate the phenotype. Clin Dysmorphol (2012) 1.41
Pediatric liver transplantation: A report from a pediatric surgical unit. J Indian Assoc Pediatr Surg (2011) 1.40
Hypocalcemia clinical, biochemical, radiological profile and follow-up in a tertiary hospital in India. Indian Pediatr (2002) 1.38
Breastfeeding practices and health-seeking behavior for neonatal sickness in a rural community. J Trop Pediatr (2005) 1.34
Newborn screening in India: current perspectives. Indian Pediatr (2010) 1.21
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39. Am J Hum Genet (2009) 1.21
Vitamin D deficiency in healthy breastfed term infants at 3 months & their mothers in India: seasonal variation & determinants. Indian J Med Res (2011) 1.16
Further characterization of ATP6V0A2-related autosomal recessive cutis laxa. Hum Genet (2012) 1.15
Poly (propyleneimine) dendrimer based nanocontainers for targeting of efavirenz to human monocytes/macrophages in vitro. J Drug Target (2007) 1.14
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness. Am J Hum Genet (2005) 1.10
Hand-foot-and-mouth disease in Calicut. Indian J Pediatr (2005) 1.09
Humanized care of preterm babies. Indian Pediatr (2003) 1.08
Topical umbilical cord care. Pediatr Infect Dis J (2013) 1.07
Intravenous fluid regimen and hyponatraemia among children: a randomized controlled trial. Pediatr Nephrol (2010) 1.07
Acute renal failure in neonates. Indian J Pediatr (2008) 1.02
Clinical profile and frequency of delta f508 mutation in Indian children with cystic fibrosis. Indian Pediatr (2003) 1.01
Schinzel acrocallosal syndrome. Indian J Pediatr (2003) 1.01
Carbimazole embryopathy-bilateral choanal atresia and patent vitello-intestinal duct: a case report and review of literature. Birth Defects Res A Clin Mol Teratol (2008) 1.01
Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa. Mol Genet Metab (2013) 1.00
Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases. Mol Cytogenet (2008) 0.99
Bubble vs conventional continuous positive airway pressure for prevention of extubation failure in preterm very low birth weight infants: a pilot study. Indian J Pediatr (2011) 0.97
Conducting continuing medical education program. Indian Pediatr (2002) 0.95
Griscelli syndrome. J Am Acad Dermatol (2006) 0.95
Factor VII Deficiency: A Rare Case Report. Indian J Hematol Blood Transfus (2010) 0.95
Thrombocytopenic purpura as a presenting manifestation of tubercular lymphadenitis. Indian J Pediatr (2003) 0.94
Risk factors for severe retinopathy of prematurity in preterm low birth weight neonates. Indian J Pediatr (2011) 0.93
Retinopathy of prematurity. Indian J Pediatr (2008) 0.93
Pyle metaphyseal dysplasia. Indian Pediatr (2008) 0.93
Microbiological study of neonatal conjunctivitis with special reference to Chlamydia trachomatis. Indian J Ophthalmol (2002) 0.93
Precocious puberty: clinical and endocrine profile and factors indicating neurogenic precocity in Indian children. J Pediatr Endocrinol Metab (2002) 0.91
Velaglucerase alfa enzyme replacement therapy compared with imiglucerase in patients with Gaucher disease. Am J Hematol (2013) 0.91
Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders. Fertil Steril (2003) 0.91
Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. Am J Med Genet A (2003) 0.90
Hydroxyurea in thalassemia intermedia--a promising therapy. Ann Hematol (2005) 0.89
Ovarian cysts in young girls with hypothyroidism: follow-up and effect of treatment. J Pediatr Endocrinol Metab (2006) 0.89
Feeding behaviour and performance of preterm neonates on Paladai feeding. Acta Paediatr (2013) 0.89
Prevalence of MTHFR C677T polymorphism in north Indian mothers having babies with Trisomy 21 Down syndrome. Downs Syndr Res Pract (2008) 0.88
Transfusion related acute lung injury in a neonate. Indian J Pediatr (2011) 0.88
Intranasal versus intravenous lorazepam for control of acute seizures in children: a randomized open-label study. Epilepsia (2011) 0.87
Early skin-to-skin contact and breast-feeding behavior in term neonates: a randomized controlled trial. Neonatology (2012) 0.87
Hypomelanosis of Ito with hemimegalencephaly. Dermatol Online J (2009) 0.87
Retinopathy of prematurity screening by non-retinologists. Indian J Pediatr (2006) 0.87
Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India. BMC Med Genet (2010) 0.87
Trial of daily vitamin D supplementation in preterm infants. Pediatrics (2014) 0.86
Intellectual disability in Indian children: experience with a stratified approach for etiological diagnosis. Indian Pediatr (2013) 0.86
Hypoglycemia in the newborn. Indian J Pediatr (2010) 0.86
Management of neonatal seizures. Indian J Pediatr (2010) 0.86
Vitamin A responsive night blindness in Dent's disease. Pediatr Nephrol (2009) 0.86
Carrier frequency of F508del mutation of cystic fibrosis in Indian population. J Cyst Fibros (2005) 0.85
Perinatal HIV. Indian J Pediatr (2008) 0.85
Seizures in the newborn. Indian J Pediatr (2008) 0.85
Epilepsy in children with Down syndrome. Epileptic Disord (2011) 0.85
Changing profile of retinopathy of prematurity. J Trop Pediatr (2002) 0.85
Prenatal diagnosis of fetal peters' plus syndrome: a case report. Case Rep Genet (2013) 0.85
Clinical profile and mutation analysis of xeroderma pigmentosum in Indian patients. Indian J Dermatol Venereol Leprol (2015) 0.85
Kangaroo mother care--an alternative to conventional care. Indian J Pediatr (2008) 0.85
Detection of 22 q11.2 hemizygous deletion by interphase FISH in a patient with features of CATCH 22 syndrome. Indian Pediatr (2005) 0.85
Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India. Hum Mutat (2013) 0.85
Prevalence of celiac disease in Indian children with Down syndrome and its clinical and laboratory predictors. Indian J Pediatr (2012) 0.84
Survival and morbidity in extremely low birth weight (ELBW) infants. Indian Pediatr (2003) 0.84