| Bobbi Jeanne Honkomp, ARNP | |
|
1200 1st Ave E, Suite B, Spencer, IA 51301-4342 | |
| (712) 262-6214 | |
| (712) 262-6216 |
| Full Name | Bobbi Jeanne Honkomp |
|---|---|
| Gender | Female |
| Speciality | Nurse Practitioner |
| Experience | 13 Years |
| Location | 1200 1st Ave E, Spencer, Iowa |
| Accepts Medicare Assignments | Yes. She accepts the Medicare-approved amount; you will not be billed for any more than the Medicare deductible and coinsurance. |
| Identifier | Type | State | Issuer |
|---|---|---|---|
| 1649568825 | NPI | - | NPPES |
| Taxonomy | Type | License (State) | Status |
|---|---|---|---|
| 363L00000X | Nurse Practitioner | A098436 (Iowa) | Primary |
| Facility Name | Location | Facility Type |
|---|---|---|
| Spencer Municipal Hospital | Spencer, IA | Hospital |
| Pocahontas Community Hospital | Pocahontas, IA | Hospital |
| Avera Holy Family Hospital | Estherville, IA | Hospital |
| Lakes Regional Healthcare | Spirit lake, IA | Hospital |
| Palo Alto County Hospital | Emmetsburg, IA | Hospital |
| Group Practice Name | Group PECOS PAC ID | No. of Members |
|---|---|---|
| Northwest Iowa Urologists Pc | 4587554670 | 3 |
News Archive
The laboratory of Huda Zoghbi, where the discovery that mutations in the gene MECP2 cause the severe childhood neurological disorder Rett Syndrome was made, has taken yet another step toward unraveling the complex epigenetic functions of this gene, implicated also in cases of autism, bipolar disease and childhood onset schizophrenia. The November 11 issue of Nature reports that removing MECP2 from a small group of neurons that typically make the inhibitory neurotransmitter, GABA, recapitulates many symptoms of Rett as well as numerous neuropsychiatric disorders.
Loyola Medicine is enrolling patients in a landmark clinical trial of a new procedure to treat atrial fibrillation, the most common type of irregular heartbeat.
The cellular cause of birth defects like cleft palates, missing teeth and problems with fingers and toes has been a tricky puzzle for scientists. Now Professor Emily Bates and her biochemistry students at Brigham Young University have placed an important piece of the developmental puzzle. They studied an ion channel that regulates the electrical charge of a cell. In a new study published by the journal Development, they show that blocking this channel disrupts the work of a protein that is supposed to carry marching orders to the nucleus.
Researchers suggest a possible cell-based therapy to stimulate lung development in fragile premature infants who suffer from a rare condition called Bronchopulmonary Dysplasia, which in the most severe cases can lead to lifelong breathing problems and even death.
› Verified 8 days ago
| Entity Name | Northwest Iowa Urologists Pc |
|---|---|
| Entity Type | Part B Supplier - Clinic/group Practice |
| Entity Identifiers | NPI Number: 1063465003 PECOS PAC ID: 4587554670 Enrollment ID: O20040319001469 |
News Archive
The laboratory of Huda Zoghbi, where the discovery that mutations in the gene MECP2 cause the severe childhood neurological disorder Rett Syndrome was made, has taken yet another step toward unraveling the complex epigenetic functions of this gene, implicated also in cases of autism, bipolar disease and childhood onset schizophrenia. The November 11 issue of Nature reports that removing MECP2 from a small group of neurons that typically make the inhibitory neurotransmitter, GABA, recapitulates many symptoms of Rett as well as numerous neuropsychiatric disorders.
Loyola Medicine is enrolling patients in a landmark clinical trial of a new procedure to treat atrial fibrillation, the most common type of irregular heartbeat.
The cellular cause of birth defects like cleft palates, missing teeth and problems with fingers and toes has been a tricky puzzle for scientists. Now Professor Emily Bates and her biochemistry students at Brigham Young University have placed an important piece of the developmental puzzle. They studied an ion channel that regulates the electrical charge of a cell. In a new study published by the journal Development, they show that blocking this channel disrupts the work of a protein that is supposed to carry marching orders to the nucleus.
Researchers suggest a possible cell-based therapy to stimulate lung development in fragile premature infants who suffer from a rare condition called Bronchopulmonary Dysplasia, which in the most severe cases can lead to lifelong breathing problems and even death.
› Verified 8 days ago
| Mailing Address | Practice Location Address |
|---|---|
| Bobbi Jeanne Honkomp, ARNP 1200 1st Ave E, Suite B, Spencer, IA 51301-4342 Ph: (712) 262-6214 | Bobbi Jeanne Honkomp, ARNP 1200 1st Ave E, Suite B, Spencer, IA 51301-4342 Ph: (712) 262-6214 |
News Archive
The laboratory of Huda Zoghbi, where the discovery that mutations in the gene MECP2 cause the severe childhood neurological disorder Rett Syndrome was made, has taken yet another step toward unraveling the complex epigenetic functions of this gene, implicated also in cases of autism, bipolar disease and childhood onset schizophrenia. The November 11 issue of Nature reports that removing MECP2 from a small group of neurons that typically make the inhibitory neurotransmitter, GABA, recapitulates many symptoms of Rett as well as numerous neuropsychiatric disorders.
Loyola Medicine is enrolling patients in a landmark clinical trial of a new procedure to treat atrial fibrillation, the most common type of irregular heartbeat.
The cellular cause of birth defects like cleft palates, missing teeth and problems with fingers and toes has been a tricky puzzle for scientists. Now Professor Emily Bates and her biochemistry students at Brigham Young University have placed an important piece of the developmental puzzle. They studied an ion channel that regulates the electrical charge of a cell. In a new study published by the journal Development, they show that blocking this channel disrupts the work of a protein that is supposed to carry marching orders to the nucleus.
Researchers suggest a possible cell-based therapy to stimulate lung development in fragile premature infants who suffer from a rare condition called Bronchopulmonary Dysplasia, which in the most severe cases can lead to lifelong breathing problems and even death.
› Verified 8 days ago
Kathi Kae Heckert, CNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 116 E 11th St, Ste 101, Spencer, IA 51301 Phone: 712-264-3500 Fax: 712-264-3535 | |
Sara Casey, ARNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 116 E 11th St, Spencer, IA 51301 Phone: 712-264-3500 | |
Kimberly Goslinga, ARNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 201 E 11th St, Spencer, IA 51301 Phone: 800-242-5101 | |
Jill A. Hustedt, ARNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 337 11th St Sw, Spencer, IA 51301 Phone: 712-792-7500 Fax: 712-792-7510 | |
Leisha Fischer, ARNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 116 East 7th Street, Suite 2, Spencer, IA 51301 Phone: 712-580-6592 Fax: 712-580-6593 | |
Kathryn S Nelson, ARNP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 337 11th St Sw, Spencer, IA 51301 Phone: 712-580-4570 Fax: 712-580-4573 | |
Ms. Kimberly Whisenant, NP Nurse Practitioner Medicare: Accepting Medicare Assignments Practice Location: 116 E 11th St Ste 101, Spencer, IA 51301 Phone: 712-264-3500 Fax: 712-264-3525 |