Kristen Ferreira Lcsw | |
47 Reckless Pl Red Bank NJ 07701-1750 | |
(908) 447-2846 | |
Not Available |
Full Name | Kristen Ferreira Lcsw |
---|---|
Speciality | Social Worker - Clinical |
Location | 47 Reckless Pl, Red Bank, New Jersey |
Authorized Official Name and Position | Kristen Ferreira (CLINICIAN) |
Authorized Official Contact | 9084472846 |
Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
Mailing Address | Practice Location Address |
---|---|
Kristen Ferreira Lcsw 47 Reckless Pl Red Bank NJ 07701-1750 Ph: () - | Kristen Ferreira Lcsw 47 Reckless Pl Red Bank NJ 07701-1750 Ph: (908) 447-2846 |
NPI Number | 1033477708 |
---|---|
Provider Enumeration Date | 05/01/2012 |
Last Update Date | 05/01/2012 |
Identifier | Type | State | Issuer |
---|---|---|---|
1033477708 | NPI | - | NPPES |
Taxonomy | Type | License (State) | Status |
---|---|---|---|
1041C0700X | Social Worker - Clinical | (* (Not Available)) | Primary |
News Archive
Cancer of the throat and mouth (oropharyngeal cancers, OPC) are common, and are increasing in incidence especially among younger people. However, these are difficult to diagnose as they are not seen either by the patient or during routine medical examinations.
Asthma in children is on the rise worldwide and scientists have often blamed the environment for this trend. Britain has more than 1.1 million children and the US has nearly 10 million children with asthma. In a new international study diet has been cited to be a factor that affects asthma in children. The study on Allergies and Asthma in Childhood has shown what many parents knew for a while now – burgers are not good for children.
San Francisco-based Nuvon, Inc. (www.nuvon.com), a provider of next generation BMDI (biomedical device interoperability) solutions, announces the introduction of the IDM-MG 1000, extending Nuvon's biomedical device interoperability capabilities by providing the first truly mobile and portable solution to collect and present critical biomedical device data anywhere.
Endologix, Inc., developer of minimally invasive treatments for aortic disorders, announced today that it has received U.S. Food and Drug Administration (FDA) approval for its expanded offering of Powerlink® stent graft products. The approval covers 31 new sizes of Powerlink® main body bifurcated, proximal extension, and limb extension stent grafts that increase the system's addressable patient population by 5% to 10%.
Early intervention services for children with disabilities or developmental delays are focused on being family centered and are ideally conducted in the home setting. Even so, fathers—custodial or noncustodial—are often left out of the process.
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