Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1983 1
1987 2
1988 1
1990 1
1993 1
1994 2
1995 1
1996 2
1997 1
1998 3
1999 1
2000 1
2001 1
2002 3
2004 2
2005 2
2006 2
2007 2
2008 1
2009 1
2010 2
2011 1
2012 1
2015 1
2017 2
2018 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

40 results

Results by year

Filters applied: . Clear all
Page 1
Donohue syndrome: A review of literature, case series, and anesthetic considerations.
Kirkwood A, Stuart G, Harding L. Kirkwood A, et al. Paediatr Anaesth. 2018 Jan;28(1):23-27. doi: 10.1111/pan.13273. Epub 2017 Nov 17. Paediatr Anaesth. 2018. PMID: 29148123 Review.
BACKGROUND: Donohue syndrome is a rare autosomal recessive disorder of insulin resistance, causing a functional defect in insulin receptor function, and affecting the ability of the insulin to bind the receptor. ...DISCUSSION: There is currently no published literat …
BACKGROUND: Donohue syndrome is a rare autosomal recessive disorder of insulin resistance, causing a functional defect in insu …
IGF-I treatment of insulin resistance.
McDonald A, Williams RM, Regan FM, Semple RK, Dunger DB. McDonald A, et al. Eur J Endocrinol. 2007 Aug;157 Suppl 1:S51-6. doi: 10.1530/EJE-07-0271. Eur J Endocrinol. 2007. PMID: 17785698 Review.
Severe insulin resistance resulting from known or putative genetic defects affecting the insulin receptor or post-insulin receptor signalling represents a clinical spectrum ranging from Donohue's and Rabson-Mendenhall syndrome, where the genetic defect is identified …
Severe insulin resistance resulting from known or putative genetic defects affecting the insulin receptor or post-insulin receptor signallin …
Rabson-Mendenhall syndrome: two case reports and a brief review of the literature.
Bathi RJ, Parveen S, Mutalik S, Rao R. Bathi RJ, et al. Odontology. 2010 Feb;98(1):89-96. doi: 10.1007/s10266-009-0106-7. Epub 2010 Feb 16. Odontology. 2010. PMID: 20155514 Review.
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder characterized by insulin resistance syndrome, growth retardation, coarse and senile-looking faces, mental precocity, early dentition, and pineal hyperplasia. Mutations of the insulin receptor gene af …
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder characterized by insulin resistance syndrome, growth retard …
Insulin receptor disorders in Japan.
Kasuga M, Kadowaki T. Kasuga M, et al. Diabetes Res Clin Pract. 1994 Oct;24 Suppl:S145-51. doi: 10.1016/0168-8227(94)90242-9. Diabetes Res Clin Pract. 1994. PMID: 7859597 Review.
The clinical features of insulin receptor disorders found in Japan are summarized. About 20 cases of primary receptor mutations (type A syndrome of insulin resistance, leprechaunism and Rabson-Mendenhall syndrome) and 16 cases of autoantibodies against insuli …
The clinical features of insulin receptor disorders found in Japan are summarized. About 20 cases of primary receptor mutations (type A s …
[Monogenic severe insulin resistance syndromes].
Vincent-Desplanques D, Faivre-Defrance F, Wémeau JL, Vantyghem MC. Vincent-Desplanques D, et al. Rev Med Interne. 2005 Nov;26(11):866-73. doi: 10.1016/j.revmed.2005.04.027. Rev Med Interne. 2005. PMID: 15908053 Review. French.
The clinical and biological presentation is similar to that one of metabolic syndrome. Polycystic ovaries syndrome, non-alcoholic liver steatosis, acanthosis nigricans and overall, lipo-atrophic syndrome must be sought. Genetically determined forms are mainly …
The clinical and biological presentation is similar to that one of metabolic syndrome. Polycystic ovaries syndrome, non-alcoho …
Leprechaunism: report of two cases and review.
Ioan D, Dumitriu L, Belengeanu V, Bistriceanu M, Maximilian C. Ioan D, et al. Endocrinologie. 1988 Jul-Sep;26(3):205-9. Endocrinologie. 1988. PMID: 3062757 Review.
Two new cases of leprechaunism are reported, one of which from consanguinous parents. ...Endocrinologically, one of the patients shows the syndrome of low T3. The role of the endocrine alterations in the etiology of the syndrome is discussed....
Two new cases of leprechaunism are reported, one of which from consanguinous parents. ...Endocrinologically, one of the patients show …
Alcohol, microbiome, life style influence alcohol and non-alcoholic organ damage.
Neuman MG, French SW, Zakhari S, Malnick S, Seitz HK, Cohen LB, Salaspuro M, Voinea-Griffin A, Barasch A, Kirpich IA, Thomes PG, Schrum LW, Donohue TM Jr, Kharbanda KK, Cruz M, Opris M. Neuman MG, et al. Exp Mol Pathol. 2017 Feb;102(1):162-180. doi: 10.1016/j.yexmp.2017.01.003. Epub 2017 Jan 7. Exp Mol Pathol. 2017. PMID: 28077318 Free article. Review.
Dietary interventions such as micro and macronutrients, as well as changes to the microbiota have been suggested. The clinical aspects of NASH, as part of the metabolic syndrome in the aging population, have been presented. The symposium addressed mechanisms and biomarkers …
Dietary interventions such as micro and macronutrients, as well as changes to the microbiota have been suggested. The clinical aspects of NA …
Inhaled nitric oxide in preterm infants: a systematic review.
Donohue PK, Gilmore MM, Cristofalo E, Wilson RF, Weiner JZ, Lau BD, Robinson KA, Allen MC. Donohue PK, et al. Pediatrics. 2011 Feb;127(2):e414-22. doi: 10.1542/peds.2010-3428. Epub 2011 Jan 10. Pediatrics. 2011. PMID: 21220391 Review.
[A rare polydysmorphic syndrome: leprechaunism. Review of 49 cases reported in the literature].
Cantani A, Ziruolo MG, Tacconi ML. Cantani A, et al. Ann Genet. 1987;30(4):221-7. Ann Genet. 1987. PMID: 3322162 Review. French.
Leprechaunism is a very rare condition of obscure etiology. Since the first report (Donohue, 1948) 48 patients have been described. ...After reviewing the literature and discussing the morphological, biological, and etiopathogenetic aspects, the authors conclude tha …
Leprechaunism is a very rare condition of obscure etiology. Since the first report (Donohue, 1948) 48 patients have been descr …
40 results