Suchergebnisse - "Patel, Mitali"

PubPharm (71)

51

Corrigendum : TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

enthalten in: Nature communications | 2016

von Schmidts, M. | Hou, Y. | Cortés, C. | +25

ErratumFor: Nat Commun. 2015;6:7074. - PMID 26044572

52

Preparation and in vitro/ex vivo evaluation of nanoemulsion for transnasal delivery of paliperidone

enthalten in: Applied nanoscience | 2016

von Patel, M. | Patel, M. | Patel, R.

53

Preparation and in vitro/ex vivo evaluation of nanoemulsion for transnasal delivery of paliperidone

enthalten in: Applied nanoscience | 2016

von Patel, M. | Patel, M. | Patel, R.

54

Submicron Emulsions and Their Applications in Oral Delivery

enthalten in: Critical reviews in therapeutic drug carrier systems | 2016

von Mundada, V. | Patel, M. | Sawant, K.

55

Cefdinir nanosuspension for improved oral bioavailability by media milling technique : formulation, characterization and in vitro-in vivo evaluations

enthalten in: Drug development and industrial pharmacy | 2016

von Sawant, K. | Patel, M. | Patel, K.

56

Cefdinir nanosuspension for improved oral bioavailability by media milling technique: formulation, characterization andin vitro–in vivoevaluations

enthalten in: Drug development and industrial pharmacy | 2016

von Sawant, K. | Patel, M. | Patel, K.

57

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

enthalten in: Nature communications | 2015

von Schmidts, M. | Hou, Y. | Cortés, C. | +125

ErratumIn: Nat Commun. 2016;7:11270. - PMID 27021811

58

Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

enthalten in: Human molecular genetics | 2014

von Onoufriadis, A. | Shoemark, A. | Schmidts, M. | +21

59

Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

enthalten in: Human molecular genetics | 2014

von Onoufriadis, A. | Shoemark, A. | Schmidts, M. | +21

60

A novel CFHR5 fusion protein causes C3 glomerulopathy in a family without Cypriot ancestry

enthalten in: Kidney international | 2014

von Medjeral-Thomas, N. | Malik, T. | Patel, M. | +4