Hypoglossia-Hypodactyly Syndrome with Short Stature - A Case Report

Por Goyal, Manisha, Singh, Ankur, Singh, Pratiksha, Kapoor, Seema
Publicado em 2014

Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation

Por Goyal, Manisha, Pradhan, Gaurav, Gupta, Sunita, Kapoor, Seema
Publicado no Contemp Clin Dent (2015)

The Diagnostic Dilemma of Cutis Laxa: A Report of Two Cases with Genotypic Dissimilarity

Por Goyal, Manisha, Singh, Ankur, Kornak, Uwe, Kapoor, Seema
Publicado no Indian J Dermatol (2015)

Stickler Syndrome Type 1 with Short Stature and Atypical Ocular Manifestations

Por Goyal, Manisha, Kapoor, Seema, Ikegawa, Shiro, Nishimura, Gen
Publicado no Case Rep Pediatr (2016)

Role of different media in Karpanpatru Taila preparation

Por Goyal, Manisha, Patgiri, B. J., Ravishankar, B., Prajapati, P. K.
Publicado em 2010

Fetal Valproate Syndrome with Limb Defects: An Indian Case Report

Por Goyal, Manisha, Gupta, Ashok, Sharma, Manish, Mathur, Priyanshu, Bansal, Naresh
Publicado no Case Rep Pediatr (2016)

Infantile Onset Alexander Disease with Normal Head Circumference: A Genetically Proven Case Report

Por Goyal, Manisha, Mehndiratta, Sumit, Faruq, Mohammed, Dwivedi, Manish Kumar, Kapoor, Seema
Publicado no J Clin Diagn Res (2014)

Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome

Por Sanjeev, Rama Krishna, Kapoor, Seema, Goyal, Manisha, Kapur, Rajiv, Gleeson, Joseph Gerard
Publicado no Case Rep Pediatr (2015)

Mechanistic insights into mode of action of novel natural cathepsin L inhibitors

Por Tyagi, Chetna, Grover, Sonam, Dhanjal, Jaspreet Kaur, Goyal, Sukriti, Goyal, Manisha, Grover, Abhinav
Publicado em 2013

Development of Dual Inhibitors against Alzheimer's Disease Using Fragment-Based QSAR and Molecular Docking

Por Goyal, Manisha, Dhanjal, Jaspreet Kaur, Goyal, Sukriti, Tyagi, Chetna, Hamid, Rabia, Grover, Abhinav
Publicado em 2014

Novel Natural Structure Corrector of ApoE4 for Checking Alzheimer's Disease: Benefits from High Throughput Screening and Molecular Dynamics Simulations

Por Goyal, Manisha, Grover, Sonam, Dhanjal, Jaspreet Kaur, Goyal, Sukriti, Tyagi, Chetna, Chacko, Sajeev, Grover, Abhinav
Publicado em 2013

Molecular Diagnosis of Infantile Neuro axonal Dystrophy by Next Generation Sequencing

Por Goyal, Manisha, Bijarnia-Mahay, Sunita, Kingsmore, Stephen, Farrow, Emily, Saunders, Carol, Saxena, Renu, Verma, Ishwar C.
Publicado no Indian J Pediatr (2014)

Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome

Por Imagawa, Eri, Fukai, Ryoko, Behnam, Mahdiyeh, Goyal, Manisha, Nouri, Narges, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Salehi, Mansour, Kapoor, Seema, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi
Publicado no Hum Genome Var (2015)