ID.1
Item
women with histologically confirmed breast cancer (by core needle biopsy)
boolean
ID.2
Item
women with >= 2 cm clinically or radiologically measureable breast cancer
boolean
ID.3
Item
women scheduled to receive neoadjuvant chemotherapy as part of their treatment plan
boolean
ID.4
Item
women competent to sign study specific written informed consent
boolean
ID.5
Item
women willing to comply with protocol requirements
boolean
ID.6
Item
women who are pregnant
boolean
ID.7
Item
women who have undergone open surgical (excisional) biopsy for breast cancer diagnosis
boolean
ID.8
Item
women who have had a prior history of breast cancer in the same breast
boolean
ID.9
Item
women with known cardiac shunt, pulmonary hypertension or hypersensitivity to perflutren agent
boolean
ID.10
Item
women who cannot consent for themselves
boolean