Search Results - "STEINKRAUSS, Linda"

Defense Against Hypoglycemia: Normal Fasting Adaptation in Children by Steinkrauss, Linda J.

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The Path From Hormone Abnormality to Hypoglycemia by Steinkrauss, Linda J.

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Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2 (UCP2) by Ferrara, Christine T, Boodhansingh, Kara E, Paradies, Elenora, Giuseppe, Fiermonte, Steinkrauss, Linda J, Topor, Lisa Swartz, Quintos, Jose Bernardo, Ganguly, Arupa, De Leon, Diva D, Palmieri, Ferdinando, Stanley, Charles A

“…Context:The rarest genetic form of congenital hyperinsulinism (HI) has been associated with dominant inactivating mutations in uncoupling protein 2 (UCP2), a…”
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Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor by THORNTON, Paul S, MACMULLEN, Courtney, GANGULY, Arupa, RUCHELLI, Eduardo, STEINKRAUSS, Linda, CRANE, Ana, AGUILAR-BRYAN, Lydia, STANLEY, Charles A

“…Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor Paul…”
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Pediatric endocrinology nursing society: 2024 year in review by Steinkrauss, Linda, Keil, Meg

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Best Practices in Pediatric Endocrinology Nursing: Jenny's Story by Steinkrauss, Linda

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SUN-476 Risk of Thyroid Cancer in McCune-Albright Syndrome by Bick, Sarah L, Steinkrauss, Linda J, Thacker, Mihir M, Berman, Loren, Gannon, Anthony W

“…Abstract Background: McCune-Albright syndrome (MAS) is a well described genetic syndrome characterized by café-au-lait spots, polyostotic fibrous dysplasia,…”
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Clinical features and insulin regulation in infants with a syndrome of prolonged neonatal hyperinsulinism by Hoe, Francis M., Thornton, Paul S., Wanner, Laura A., Steinkrauss, Linda, Simmons, Rebecca A., Stanley, Charles A.

“…To characterize the clinical features and insulin regulation in infants with hypoglycemia due to prolonged neonatal hyperinsulinism. Data were collected on 26…”
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Hypoglycemia: Symptom or Diagnosis? by Halaby, Lori P., Steinkrauss, Linda

“…Hypoglycemia is analyzed with respect to diagnosis and treatment in newborns and infants as well as older children. [Copyright Elsevier B.V.]…”
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Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations by Raizen, David M., Brooks-Kayal, Amy, Steinkrauss, Linda, Tennekoon, Gihan I., Stanley, Charles A., Kelly, Andrea

“…To describe seizure phenotypes associated with the hyperinsulinism/hyperammonemia syndrome (HI/HA), which is caused by gain of function mutations in the enzyme…”
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Preoperative Evaluation of Infants with Focal or Diffuse Congenital Hyperinsulinism by Intravenous Acute Insulin Response Tests and Selective Pancreatic Arterial Calcium Stimulation by Stanley, Charles A., Thornton, Paul S., Ganguly, Arupa, MacMullen, Courtney, Underwood, Patricia, Bhatia, Pooja, Steinkrauss, Linda, Wanner, Laura, Kaye, Robin, Ruchelli, Eduardo, Suchi, Mariko, Adzick, N. Scott

“…Infants with congenital hyperinsulinism often require pancreatectomy. Recessive mutations of the ATP-dependent plasma membrane potassium channel (KATP) genes,…”
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A Fruity Case of Hypoglycemia by Steinkrauss, Linda J., Stanley, Charles A.

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Effects of Hypoglycemia on Developmental Outcome in Children With Congenital Hyperinsulinism by Steinkrauss, Linda, Lipman, Terri H., Hendell, Christine D., Gerdes, Marsha, Thornton, Paul S., Stanley, Charles A.

“…Children with congenital hyperinsulinism are at risk for recurring, severe episodes of hypoglycemia that can cause seizures, brain damage, and developmental…”
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Pregnancy in glycogen storage disease type Ib: gestational care and report of first successful deliveries by Dagli, Aditi I., Lee, Philip J., Correia, Catherine E., Rodriguez, Christina, Bhattacharya, Kaustav, Steinkrauss, Linda, Stanley, Charles A., Weinstein, David A.

“…Patients with type Ia glycogen storage disease (GSD) have been surviving well into adulthood since continuous glucose therapy was introduced in the 1970s, and…”
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Familial Leucine-Sensitive Hypoglycemia of Infancy Due to a Dominant Mutation of the β-Cell Sulfonylurea Receptor by Magge, Sheela N., Shyng, Show-Ling, MacMullen, Courtney, Steinkrauss, Linda, Ganguly, Arupa, Katz, Lorraine E. L., Stanley, Charles A.

“…Familial leucine-sensitive hypoglycemia of infancy was described in 1956 as a condition in which symptomatic hypoglycemia was provoked by protein meals or the…”
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Neonatal Diabetes: Current Trends in Diagnosis and Management by Rearson, Melissa Andrews, McKnight-Menci, Heather, Steinkrauss, Linda

“…ABSTRACTThe purpose of this article is to describe diabetes diagnosed during the first 6 months of life. Neonatal diabetes, also known as congenital diabetes,…”
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010 – No Pancreas, No Problem! A Case of Mild Diabetes After Total Pancreatectomy With Islet Autotransplantation by Linda J., Steinkrauss, Doyle, Daniel A.

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Challenges of decision making for families of children with single or multiple chronic conditions by Gruccio, D, Steinkrauss, L

“…When a child is diagnosed with a chronic illness, families begin a constant cycle of decision making. Many of these decisions surround health care treatment…”
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