Craniosynostosis genetics: The mystery unfolds

著者: Panigrahi, Inusha
出版事項 2011

A case of short stature with anterior vertebral beaking

著者: Kulkarni, Ketan Prasad, Panigrahi, Inusha
出版事項 2011

Mutational spectrum of thalassemias in India

著者: Panigrahi, Inusha, Marwaha, R. K.
出版事項 2007

Acquired syndactyly in epidermolysis bullosa dystrophica

著者: Panigrahi, Inusha, Kulkarni, Ketan, Dayal, Devi
出版事項 2009

Novel mutation in the CHST14 gene causing musculocontractural type of Ehlers-Danlos syndrome

著者: Sandal, Sapna, Kaur, Anupriya, Panigrahi, Inusha
出版年 BMJ Case Rep (2018)

Child with Mongolian spots and dysostosis multiplex

著者: Kulkarni, Ketan Prasad, Murthy, Srinivasa, Panigrahi, Inusha
出版事項 2009

MOMO Syndrome with Holoprosencephaly and Cryptorchidism: Expanding the Spectrum of the New Obesity Syndrome

著者: Sharda, Sheetal, Panigrahi, Inusha, Marwaha, Ram Kumar
出版事項 2011

KLHL40 Mutation Associated with Severe Nemaline Myopathy, Fetal Akinesia, and Cleft Palate

著者: Avasthi, Kapil K., Agarwal, Sarita, Panigrahi, Inusha
出版年 J Pediatr Neurosci (2019)

Hemifacial microsomia with pulmonary hypoplasia

著者: Panigrahi, Inusha, Das, Rashmi Ranjan, Marwaha, Ram Kumar
出版事項 2010

Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and Diagnosis

著者: Kumar, Ravindra, Singh, Kritanjali, Panigrahi, Inusha, Agarwal, Sarita
出版事項 2013

The Effect of Prophylactic Antipyretic Administration on Post-Vaccination Adverse Reactions and Antibody Response in Children: A Systematic Review

著者: Das, Rashmi Ranjan, Panigrahi, Inusha, Naik, Sushree Samiksha
出版事項 2014

Methylmalonic Acidemia with Novel MUT Gene Mutations

著者: Panigrahi, Inusha, Bhunwal, Savita, Varma, Harish, Singh, Simranjeet
出版年 Case Rep Genet (2017)

Bardet-Biedl syndrome presenting with laryngeal web and bifid epiglottis

著者: Kaur, Parminder, Chaudhry, Chakshu, Neelam, Harsha, Panigrahi, Inusha
出版年 BMJ Case Rep (2021)

Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature

著者: Kumar, Suresh, Suthar, Renu, Panigrahi, Inusha, Marwaha, Ram K.
出版事項 2012

Hunter syndrome with persistent thrombocytopenia

著者: Panigrahi, Inusha, Dhanorkar, Manoj, Didel, Siyaram, Koganti, Raja Ashok
出版年 BMJ Case Rep (2019)

Hepatomegaly with neutropenia: a girl with glycogen storage disease Ib

著者: Bhattacharya, Deepanjan, Kumar BN, Anil, Panigrahi, Inusha, Kaur, Anupriya
出版年 BMJ Case Rep (2019)

Study of Prothrombotic Gene Variations Associated with the Risk of Development of Thrombosis in Patients with Down Syndrome

著者: Kataru, Chandreswara Raju, Krishnakumar, Vinodhini, Panigrahi, Inusha, Kannan, Meganathan
出版年 Indian J Hematol Blood Transfus (2020)

Vitamin D Supplementation for the Treatment of Acute Childhood Pneumonia: A Systematic Review

著者: Das, Rashmi Ranjan, Singh, Meenu, Panigrahi, Inusha, Naik, Sushree Samiksha
出版事項 2013

The first case report of a patient with coexisting hemophilia B and Down syndrome

著者: Rastogi, Pulkit, Kumar, Narender, Ahluwalia, Jasmina, Das, Reena, Panigrahi, Inusha
出版年 Blood Res (2017)

MTHFR promoter hypermethylation may lead to congenital heart defects in Down syndrome

著者: Asim, Ambreen, Agarwal, Sarita, Panigrahi, Inusha, Saiyed, Nazia, Bakshi, Sonal
出版年 Intractable Rare Dis Res (2017)