-
1
-
-
0025114228
-
Persistent hyperinsulinemic hypoglycemia of infancy (“nesidioblastosis”): autosomal recessive inheritance in 7 pedigrees
-
B Glaser M Phillip R Carmi E Lieberman H Landau Persistent hyperinsulinemic hypoglycemia of infancy (“nesidioblastosis”): autosomal recessive inheritance in 7 pedigrees Am J Med Genet 37 1990 511 515
-
(1990)
Am J Med Genet
, vol.37
, pp. 511-515
-
-
Glaser, B1
Phillip, M2
Carmi, R3
Lieberman, E4
Landau, H5
-
3
-
-
0026053121
-
Familial and sporadic hyperinsulinism: histopathology and segregation analysis support a single autosomal recessive disorder
-
PS Thornton AE Sumner ED Ruchelli RS Spielman L Baker CA Stanley Familial and sporadic hyperinsulinism: histopathology and segregation analysis support a single autosomal recessive disorder J Pediatr 119 1991 721 724
-
(1991)
J Pediatr
, vol.119
, pp. 721-724
-
-
Thornton, PS1
Sumner, AE2
Ruchelli, ED3
Spielman, RS4
Baker, L5
Stanley, CA6
-
4
-
-
0028236583
-
Familial hyperinsulinism maps to human chromosome 11p 14-15, 30 cM centromeric to the insulin gene
-
B Glaser KC Chiu R Anker Familial hyperinsulinism maps to human chromosome 11p 14-15, 30 cM centromeric to the insulin gene Nat Genet 7 1994 185 188
-
(1994)
Nat Genet
, vol.7
, pp. 185-188
-
-
Glaser, B1
Chiu, KC2
Anker, R3
-
5
-
-
0028801579
-
Homozygosity mapping to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy
-
PM Thomas GJ Cote DM Hallman PM Mathew Homozygosity mapping to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy Am J Hum Genet 56 1995 416 421
-
(1995)
Am J Hum Genet
, vol.56
, pp. 416-421
-
-
Thomas, PM1
Cote, GJ2
Hallman, DM3
Mathew, PM4
-
6
-
-
0029024314
-
Cloning of the beta cell high affinity sulfonylurea receptor: a regulator of insulin secretion
-
L Aguilar-Bryan CG Nichols SW Wechsler Cloning of the beta cell high affinity sulfonylurea receptor: a regulator of insulin secretion Science 268 1995 423 426
-
(1995)
Science
, vol.268
, pp. 423-426
-
-
Aguilar-Bryan, L1
Nichols, CG2
Wechsler, SW3
-
7
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
PM Thomas GJ Cote N Wohlik Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy Science 268 1995 426 429
-
(1995)
Science
, vol.268
, pp. 426-429
-
-
Thomas, PM1
Cote, GJ2
Wohlik, N3
-
9
-
-
0027374336
-
Acute and long term treatment of congenital hyperinsulinism with octreotide
-
PS Thornton CA Alter LE Levit Katz L Baker CA Stanley Acute and long term treatment of congenital hyperinsulinism with octreotide J Pediatr 123 1993 637 643
-
(1993)
J Pediatr
, vol.123
, pp. 637-643
-
-
Thornton, PS1
Alter, CA2
Levit Katz, LE3
Baker, L4
Stanley, CA5
-
10
-
-
85119465917
-
Use of a highly sensitive assay to document elevated insulin levels in congenital hyperinsulinism [abstract]
-
M Satin Smith LE Levitt-Katz H Drott Use of a highly sensitive assay to document elevated insulin levels in congenital hyperinsulinism [abstract] Pediatr Res 37 1996 100A
-
(1996)
Pediatr Res
, vol.37
, pp. 100A
-
-
Satin Smith, M1
Levitt-Katz, LE2
Drott, H3
-
11
-
-
0017278130
-
Hyperinsulinism in infants and children: diagnosis and therapy
-
CA Stanley L Baker Hyperinsulinism in infants and children: diagnosis and therapy Adv Pediatr 23 1976 315 355
-
(1976)
Adv Pediatr
, vol.23
, pp. 315-355
-
-
Stanley, CA1
Baker, L2
-
12
-
-
0025293368
-
Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci
-
JL Weber AE Kwitek PE May Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci Nucleic Acids Res 18 1990 4036
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 4036
-
-
Weber, JL1
Kwitek, AE2
May, PE3
-
13
-
-
0026736249
-
Isolation and chromosomal assignment of 100 highly informative human single sequence repeat polymorphisms
-
TJ Hudson M Engelstein MK Lee Isolation and chromosomal assignment of 100 highly informative human single sequence repeat polymorphisms Genomics 13 1992 622 629
-
(1992)
Genomics
, vol.13
, pp. 622-629
-
-
Hudson, TJ1
Engelstein, M2
Lee, MK3
-
15
-
-
0030036875
-
Molecular biology of the beta cell ATP sensitive K+ channel
-
S Seino N Inagaki N Namba T Gonoi Molecular biology of the beta cell ATP sensitive K+ channel Diabetes Rev 4 1996 177 190
-
(1996)
Diabetes Rev
, vol.4
, pp. 177-190
-
-
Seino, S1
Inagaki, N2
Namba, N3
Gonoi, T4
-
17
-
-
0001395189
-
Leucine induced hypoglycemia: a review and speculations
-
AM DiGeorge VH Auerbach Leucine induced hypoglycemia: a review and speculations Am J Med Sci 240 1960 792 801
-
(1960)
Am J Med Sci
, vol.240
, pp. 792-801
-
-
DiGeorge, AM1
Auerbach, VH2
-
18
-
-
16044362876
-
Symptomatic leucine sensitivity in a mother and daughter
-
AJ Ebbin C Huntley RE Tranquada Symptomatic leucine sensitivity in a mother and daughter Metabolism 16 1967 926 932
-
(1967)
Metabolism
, vol.16
, pp. 926-932
-
-
Ebbin, AJ1
Huntley, C2
Tranquada, RE3
-
19
-
-
7144237767
-
Familial hyperinsulinism (HI) inherited in an autosomal dominant (AD) form differs clinically and genetically from the more common autosomal recessive (AR) form [abstract]
-
PS Thornton B Glaser K Herold Familial hyperinsulinism (HI) inherited in an autosomal dominant (AD) form differs clinically and genetically from the more common autosomal recessive (AR) form [abstract] Pediatr Res 37 1995 100A
-
(1995)
Pediatr Res
, vol.37
, pp. 100A
-
-
Thornton, PS1
Glaser, B2
Herold, K3
-
20
-
-
0030936044
-
An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus
-
A Kukuvitis C Deal L Arbour C Polychronakos An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus J Endocrinol Metab 82 1997 1192 1194
-
(1997)
J Endocrinol Metab
, vol.82
, pp. 1192-1194
-
-
Kukuvitis, A1
Deal, C2
Arbour, L3
Polychronakos, C4
-
21
-
-
0017687811
-
Familial islet-cell adenomatosis
-
KH Tragl WR Mayr Familial islet-cell adenomatosis Lancet 2 1977 426 428
-
(1977)
Lancet
, vol.2
, pp. 426-428
-
-
Tragl, KH1
Mayr, WR2
-
22
-
-
0018851716
-
Pancreatic pathology in hyperinsulinemic hypoglycemia of infancy
-
R Jaffe Y Hashida EJ Yunis Pancreatic pathology in hyperinsulinemic hypoglycemia of infancy Lab Invest 42 1980 356 365
-
(1980)
Lab Invest
, vol.42
, pp. 356-365
-
-
Jaffe, R1
Hashida, Y2
Yunis, EJ3
-
23
-
-
0023786661
-
Changing concepts of islet cell dysplasia in neonatal and infantile hyperinsulinism
-
CG Thomas RE Cuenca RG Azizkhan LE Underwood CN Carney Changing concepts of islet cell dysplasia in neonatal and infantile hyperinsulinism World J Surg 12 1988 598 609
-
(1988)
World J Surg
, vol.12
, pp. 598-609
-
-
Thomas, CG1
Cuenca, RE2
Azizkhan, RG3
Underwood, LE4
Carney, CN5
-
24
-
-
0024545488
-
Relevance of endocrine pancreas nesidioblastosis to hyperinsulinemic hypoglycemia
-
J Rahier Relevance of endocrine pancreas nesidioblastosis to hyperinsulinemic hypoglycemia Diabetes Care 12 1989 164 166
-
(1989)
Diabetes Care
, vol.12
, pp. 164-166
-
-
Rahier, J1
-
25
-
-
0019777591
-
Nesidioblastosis associated with insulin mediated hypoglycemia in an adult
-
DM Nathan L Axelrod KH Proppe Nesidioblastosis associated with insulin mediated hypoglycemia in an adult Diabetes Care 4 1981 383 388
-
(1981)
Diabetes Care
, vol.4
, pp. 383-388
-
-
Nathan, DM1
Axelrod, L2
Proppe, KH3
-
26
-
-
0022616877
-
Islet cell hyperplasia: an unusual cause of hypoglycemia in an adult
-
G Weinstock P Marguiles E Kahn M Susin G Abrams Islet cell hyperplasia: an unusual cause of hypoglycemia in an adult Metabolism 35 1986 110 117
-
(1986)
Metabolism
, vol.35
, pp. 110-117
-
-
Weinstock, G1
Marguiles, P2
Kahn, E3
Susin, M4
Abrams, G5
-
27
-
-
0025161909
-
Adult onset nesidioblastosis: response of glucose, insulin, and secondary peptides to therapy with sandostatin
-
EJ Mozell EA Woltering TM O’Dorisio Adult onset nesidioblastosis: response of glucose, insulin, and secondary peptides to therapy with sandostatin Am J Gastroenterol 85 1990 181 188
-
(1990)
Am J Gastroenterol
, vol.85
, pp. 181-188
-
-
Mozell, EJ1
Woltering, EA2
O’Dorisio, TM3
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