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Guidance programme

Showing 726 to 750 of 1866

Published guidance, NICE advice and quality standards
TitleReference numberPublishedLast updated
Indoor air quality at homeNG149
Cannabidiol with clobazam for treating seizures associated with Dravet syndromeTA614
Cannabidiol with clobazam for treating seizures associated with Lennox–Gastaut syndromeTA615
Balloon dilation for chronic eustachian tube dysfunctionIPG665
Menopause: diagnosis and managementNG23
gammaCore for cluster headacheMTG46
Cerliponase alfa for treating neuronal ceroid lipofuscinosis type 2HST12
Irreversible electroporation for primary liver cancerIPG664
Diverticular disease: diagnosis and managementNG147
Neratinib for extended adjuvant treatment of hormone receptor-positive, HER2-positive early stage breast cancer after adjuvant trastuzumabTA612
Workplace health: long-term sickness absence and capability to workNG146
Pentosan polysulfate sodium for treating bladder pain syndromeTA610
Rucaparib for maintenance treatment of relapsed platinum-sensitive ovarian, fallopian tube or peritoneal cancerTA611
Point-of-care creatinine devices to assess kidney function before CT imaging with intravenous contrastDG37
Rapid tests for group A streptococcal infections in people with a sore throatDG38
Ibrutinib with rituximab for treating Waldenstrom's macroglobulinaemia (terminated appraisal)TA608
Ramucirumab for treating unresectable hepatocellular carcinoma after sorafenib (terminated appraisal)TA609
Gastro-oesophageal reflux disease and dyspepsia in adults: investigation and managementCG184
Rivaroxaban for preventing atherothrombotic events in people with coronary or peripheral artery diseaseTA607
Lanadelumab for preventing recurrent attacks of hereditary angioedemaTA606
Midcarpal hemiarthroplasty for wrist arthritisIPG663
End of life care for adults: service deliveryNG142
Diabetic foot problems: prevention and managementNG19
Xeomin (botulinum neurotoxin type A) for treating chronic sialorrhoeaTA605
Voretigene neparvovec for treating inherited retinal dystrophies caused by RPE65 gene mutationsHST11

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