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Items: 1 to 50 of 55

1.

Two Cases of Pulmonary Hypertension Associated with Type III Glycogen Storage Disease.

Lee TM, Berman-Rosenzweig ES, Slonim AE, Chung WK.

JIMD Rep. 2011;1:79-82. doi: 10.1007/8904_2011_20. Epub 2011 Jun 22.

2.

Effect of exclusion diet with nutraceutical therapy in juvenile Crohn's disease.

Slonim AE, Grovit M, Bulone L.

J Am Coll Nutr. 2009 Jun;28(3):277-85.

PMID:
20150601
3.

Modification of the natural history of adult-onset acid maltase deficiency by nutrition and exercise therapy.

Slonim AE, Bulone L, Goldberg T, Minikes J, Slonim E, Galanko J, Martiniuk F.

Muscle Nerve. 2007 Jan;35(1):70-7.

PMID:
17022069
4.

Epimerase-deficiency galactosemia is not a binary condition.

Openo KK, Schulz JM, Vargas CA, Orton CS, Epstein MP, Schnur RE, Scaglia F, Berry GT, Gottesman GS, Ficicioglu C, Slonim AE, Schroer RJ, Yu C, Rangel VE, Keenan J, Lamance K, Fridovich-Keil JL.

Am J Hum Genet. 2006 Jan;78(1):89-102. Epub 2005 Nov 14.

5.

Benign course of glycogen storage disease type IIb in two brothers: nature or nurture?

Slonim AE, Bulone L, Minikes J, Hays AP, Shanske S, Tsujino S, DiMauro S.

Muscle Nerve. 2006 Apr;33(4):571-4.

PMID:
16320310
6.

Biotinidase deficiency: novel mutations and their biochemical and clinical correlates.

Wolf B, Jensen KP, Barshop B, Blitzer M, Carlson M, Goudie DR, Gokcay GH, Demirkol M, Baykal T, Demir F, Quary S, Shih LY, Pedro HF, Chen TH, Slonim AE.

Hum Mutat. 2005 Apr;25(4):413.

PMID:
15776412
7.

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.

Musumeci O, Naini A, Slonim AE, Skavin N, Hadjigeorgiou GL, Krawiecki N, Weissman BM, Tsao CY, Mendell JR, Shanske S, De Vivo DC, Hirano M, DiMauro S.

Neurology. 2001 Apr 10;56(7):849-55.

PMID:
11294920
8.

Combined biochemical and molecular diagnosis in blood of a common lipid myopathy.

Vladutiu GD, Slonim AE.

Muscle Nerve. 2000 Nov;23(11):1773-5. No abstract available.

PMID:
11054761
9.

AAEM news and comments

Vladutiu GD, Slonim AE.

Muscle Nerve. 2000 Nov;23(11):1779-84. No abstract available.

PMID:
11054762
10.

Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFR(neg) cell line.

Martiniuk F, Chen A, Donnabella V, Arvanitopoulos E, Slonim AE, Raben N, Plotz P, Rom WN.

Biochem Biophys Res Commun. 2000 Oct 5;276(3):917-23.

PMID:
11027569
11.

Identification of two subtypes of infantile acid maltase deficiency.

Slonim AE, Bulone L, Ritz S, Goldberg T, Chen A, Martiniuk F.

J Pediatr. 2000 Aug;137(2):283-5.

PMID:
10931430
12.

A preliminary study of growth hormone therapy for Crohn's disease.

Slonim AE, Bulone L, Damore MB, Goldberg T, Wingertzahn MA, McKinley MJ.

N Engl J Med. 2000 Jun 1;342(22):1633-7.

13.

Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review.

Damore ME, Speiser PW, Slonim AE, New MI, Shanske S, Xia W, Santorelli FM, DiMauro S.

J Pediatr Endocrinol Metab. 1999 Mar-Apr;12(2):207-13. Review.

PMID:
10392369
14.

Insulin-like growth factor-I and high protein diet decrease calpain-mediated proteolysis in murine muscular dystrophy.

Wingertzahn MA, Zdanowicz MM, Slonim AE.

Proc Soc Exp Biol Med. 1998 Jul;218(3):244-50.

PMID:
9648944
15.

Beneficial effect of diazoxide in obese hyperinsulinemic adults.

Alemzadeh R, Langley G, Upchurch L, Smith P, Slonim AE.

J Clin Endocrinol Metab. 1998 Jun;83(6):1911-5.

PMID:
9626118
16.

The role of dietary zinc in modifying the onset and severity of spontaneous diabetes in the BB Wistar rat.

Tobia MH, Zdanowicz MM, Wingertzahn MA, McHeffey-Atkinson B, Slonim AE, Wapnir RA.

Mol Genet Metab. 1998 Mar;63(3):205-13.

PMID:
9608543
17.

Metabolic and structural effects of insulin-like growth factor-I and high-protein diet on dystrophic hamster skeletal muscle.

Zdanowicz MM, Teichberg S, O'Connor M, Moyse J, Slonim AE.

Proc Soc Exp Biol Med. 1997 Jun;215(2):168-73.

PMID:
9160044
18.

Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death.

Santorelli FM, Schlessel JS, Slonim AE, DiMauro S.

Pediatr Neurol. 1996 Sep;15(2):145-9.

PMID:
8888049
19.

Metabolic and clinical response to recombinant human insulin-like growth factor I in myotonic dystrophy--a clinical research center study.

Vlachopapadopoulou E, Zachwieja JJ, Gertner JM, Manzione D, Bier DM, Matthews DE, Slonim AE.

J Clin Endocrinol Metab. 1995 Dec;80(12):3715-23.

PMID:
8530624
20.

Effect of insulin-like growth factor I in murine muscular dystrophy.

Zdanowicz MM, Moyse J, Wingertzahn MA, O'Connor M, Teichberg S, Slonim AE.

Endocrinology. 1995 Nov;136(11):4880-6.

PMID:
7588220
21.

High protein diet has beneficial effects in murine muscular dystrophy.

Zdanowicz MM, Slonim AE, Bilaniuk I, O'Connor MM, Moyse J, Teichberg S.

J Nutr. 1995 May;125(5):1150-8.

PMID:
7738674
22.

Nutrition therapy for hepatic glycogen storage diseases.

Goldberg T, Slonim AE.

J Am Diet Assoc. 1993 Dec;93(12):1423-30. Review.

PMID:
8245377
23.

Modification of insulin resistance by diazoxide in obese Zucker rats.

Alemzadeh R, Slonim AE, Zdanowicz MM, Maturo J.

Endocrinology. 1993 Aug;133(2):705-12.

PMID:
8344209
24.

Clinical response of alopecia, trichorrhexis nodosa, and dry, scaly skin to zinc supplementation.

Slonim AE, Sadick N, Pugliese M, Meyers-Seifer CH.

J Pediatr. 1992 Dec;121(6):890-5.

PMID:
1447651
25.

Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: pathognomonic finding of two-dimensional electrophoresis?

Harrison HH, Miller KL, Harbison MD, Slonim AE.

Clin Chem. 1992 Jul;38(7):1390-2. No abstract available.

PMID:
1623619
26.

Evaluation of the lumbar spine in patients with glycogen storage disease: CT demonstration of patterns of paraspinal muscle atrophy.

Cinnamon J, Slonim AE, Black KS, Gorey MT, Scuderi DM, Hyman RA.

AJNR Am J Neuroradiol. 1991 Nov-Dec;12(6):1099-103.

PMID:
1837202
27.

Myopathy in McArdle's syndrome. Improvement with a high-protein diet.

Slonim AE, Goans PJ.

N Engl J Med. 1985 Feb 7;312(6):355-9. No abstract available.

PMID:
3855499
28.
29.

Recurrent Reye-like syndrome: possible association with Krebs cycle abnormality.

Granot E, Deckelbaum RJ, Judd R Jr, Slonim AE, Gutman A.

Isr J Med Sci. 1984 Feb;20(2):148-52.

PMID:
6706540
30.

Chemiluminescence as an index of drug-induced free radical production in pancreatic islets.

Asayama K, English D, Slonim AE, Burr IM.

Diabetes. 1984 Feb;33(2):160-3.

PMID:
6229439
31.
32.

Nonketotic hypoglycemia: an early indicator of systemic carnitine deficiency.

Slonim AE, Borum PR, Mrak RE, Najjar J, Richardson D, Diamond MP.

Neurology. 1983 Jan;33(1):29-33.

PMID:
6681557
33.

Improvement of muscle function in acid maltase deficiency by high-protein therapy.

Slonim AE, Coleman RA, McElligot MA, Najjar J, Hirschhorn K, Labadie GU, Mrak R, Evans OB, Shipp E, Presson R.

Neurology. 1983 Jan;33(1):34-8.

PMID:
6401355
34.

Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis.

Slonim AE, Coleman RA, Moses S, Bashan N, Shipp E, Mushlin P.

Metabolism. 1983 Jan;32(1):70-4.

PMID:
6336817
35.

Hyperprolactinemia associated with advanced puberty in a male.

Slonim AE, Glick AD, Island DP, Kasselberg AG.

J Pediatr. 1982 Aug;101(2):236-9. No abstract available.

PMID:
7097420
36.

Cholesterol reduction by a high-glucose diet in a patient with homozygous familial hypercholesterolemia. A preliminary report.

Stacpoole PW, Swift LL, Greene HL, Slonim AE, Younger RK, Burr IM.

Am J Med. 1982 Jun;72(6):889-93.

PMID:
7091159
37.

Reversal of debrancher deficiency myopathy by the use of high-protein nutrition.

Slonim AE, Weisberg C, Benke P, Evans OB, Burr IM.

Ann Neurol. 1982 Apr;11(4):420-2.

PMID:
7049057
38.

Elevated cholesterol and bile acid synthesis in an adult patient with homozygous familial hypercholesterolemia. Reduction by a high glucose diet.

Stacpoole PW, Grundy SM, Swift LL, Greene HL, Slonim AE, Burr IM.

J Clin Invest. 1981 Nov;68(5):1166-71.

39.

Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infant.

Slonim AE, Borum PR, Tanaka K, Stanley CA, Kasselberg AG, Greene HL, Burr IM.

J Pediatr. 1981 Oct;99(4):551-5.

PMID:
7277094
40.

Resolution of the need for continuous nocturnal feeding in a patient with severe type I glycogen storage disease.

Greene HL, Parker PH, Slonim AE, Burr IM.

J Pediatr. 1981 Oct;99(4):602-5. No abstract available.

PMID:
6792337
41.

Regulatory role of glutathione and soluble sulfhydryl groups in the toxicity of adriamycin.

Olson RD, MacDonald JS, vanBoxtel CJ, Boerth RC, Harbison RD, Slonim AE, Freeman RW, Oates JA.

J Pharmacol Exp Ther. 1980 Nov;215(2):450-4.

PMID:
7441509
42.

Type I glycogen storage disease: five years of management with nocturnal intragastric feeding.

Greene HL, Slonim AE, Burr IM, Moran JR.

J Pediatr. 1980 Mar;96(3 Pt 2):590-5.

PMID:
6767011
43.

Protection against streptozotocin-induced diabetes by superoxide dismutase.

Robbins MJ, Sharp RA, Slonim AE, Burr IM.

Diabetologia. 1980 Jan;18(1):55-8.

PMID:
6444904
44.

Nocturnal intragastric therapy in type I glycogen storage disease: effect on hormonal and amino acid metabolism.

Slonim AE, Lacy WW, Terry A, Greene HL, Burr IM.

Metabolism. 1979 Jul;28(7):707-15.

PMID:
286865
45.

Successful treatment of severe type I glycogen storage disease with neonatal presentation by nocturnal intragastric feeding.

Perlman M, Aker M, Slonim AE.

J Pediatr. 1979 May;94(5):772-4. No abstract available.

PMID:
109590
46.

Type I glycogen storage disease: a metabolic basis for advances in treatment.

Greene HL, Slonim AE, Burr IM.

Adv Pediatr. 1979;26:63-92. Review. No abstract available.

PMID:
120680
47.

ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type I.

Greene HL, Wilson FA, Hefferan P, Terry AB, Moran JR, Slonim AE, Claus TH, Burr IM.

J Clin Invest. 1978 Aug;62(2):321-8.

48.

Improved psychological status of children under DDAVP therapy for central diabetes insipidus.

Waggoner RW Jr, Slonim AE, Armstrong SH.

Am J Psychiatry. 1978 Mar;135(3):361-2. No abstract available.

PMID:
626231
49.

Amino acid and hormonal response to long-term nocturnal nasogastric feeding therapy of glycogen storage disease type I (GSD-I).

Slonim AE, Terry A, Greene HL, Lacy WW, Burr IM.

Monogr Hum Genet. 1978;9:37-41. No abstract available.

PMID:
104149
50.

Extracellular calcium and adrenergic and cholinergic effects on islet beta-cell function.

Burr IM, Slonim AE, Burke V, Fletcher T.

Am J Physiol. 1976 Oct;231(4):1246-9.

PMID:
790976

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