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Hechtman, Peter
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Online (140)
Mediatypes
Articles (Online) (70)
Bookchapter (Online) (1)
OpenAccess-fulltext (69)
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1
The GM2 gangliosidoses datanases: Allelic variation at the ..:
Cordeiro, Paulo
;
Hechtman, Peter
;
Kaplan, Feige
Genetics in Medicine. 2 (2000) 6 - p. 319-327 , 2000
Link:
https://doi.org/10.1097/..
?
2
Variable onset of metachromatic leukodystrophy in a Vietnam..:
Arbour, Laura T
;
Silver, Kenneth
;
Hechtman, Peter
..
Pediatric Neurology. 23 (2000) 2 - p. 173-176 , 2000
Link:
https://doi.org/10.1016/..
?
3
Formation of a ternary complex between GM2 activator protei..:
Yadao, Franeli
;
Hechtman, Peter
;
Kaplan, Feige
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1340 (1997) 1 - p. 45-52 , 1997
Link:
https://doi.org/10.1016/..
?
4
Identification of Candidate Active Site Residues in Lysosom..:
Fernandes, Maria J.G.
;
Yew, Sandy
;
Leclerc, Daniel
...
Journal of Biological Chemistry. 272 (1997) 2 - p. 814-820 , 1997
Link:
https://doi.org/10.1074/..
?
5
Tay–Sachs Disease Screening and Diagnosis: Evolving Technol..:
HECHTMAN, PETER
;
KAPLAN, FEIGE
DNA and Cell Biology. 12 (1993) 8 - p. 651-665 , 1993
Link:
https://doi.org/10.1089/..
?
6
Metachromatic leukodystrophy: Multiple nonfunctional and ps..:
Francis, Gordon S.
;
Bonni, Azad
;
Shen, Ning
...
Annals of Neurology. 34 (1993) 2 - p. 212-218 , 1993
Link:
https://doi.org/10.1002/..
?
7
Prolidase deficiency: A multisystemic hereditary disorder:
Bissonnette, Robert
;
Friedmann, Dominique
;
Giroux, Jean-Mario
...
Journal of the American Academy of Dermatology. 29 (1993) 5 - p. 818-821 , 1993
Link:
https://doi.org/10.1016/..
?
8
The intron 7 donor splice site transition: a second Tay-Sac..:
Hechtman, Peter
;
Boulay, Bernard
;
De Braekeleer, Marc
...
Human Genetics. 90 (1992) 4 - p. 402-406 , 1992
Link:
https://doi.org/10.1007/..
?
9
A glycine250 → aspartate substitution in the α-subunit of h..:
Trop, Isabelle
;
Kaplan, Feige
;
Brown, Charlotte
..
Human Mutation. 1 (1992) 1 - p. 35-39 , 1992
Link:
https://doi.org/10.1002/..
?
10
Prolidase Deficiency in Cultured Human Fibroblasts: Biochem..:
Dolenga, Michael
;
Hechtman, Peter
Pediatric Research. 32 (1992) 4 - p. 479-482 , 1992
Link:
https://doi.org/10.1203/..
?
11
Specificity and sensitivity of hexosaminidase assays and DN..:
Fernandes, Maria J. G.
;
Kaplan, Feige
;
Clow, Caroline L.
...
Genetic Epidemiology. 9 (1992) 3 - p. 169-175 , 1992
Link:
https://doi.org/10.1002/..
?
12
Genetic control of ganglioside biosynthesis in mice:
Sokoloff, Dina
;
Hechtman, Peter
Biochemical Genetics. 26 (1988) 9-10 - p. 631-644 , 1988
Link:
https://doi.org/10.1007/..
?
13
Tay-Sachs disease: B1 variant:
Gordon, Bruce A.
;
Gordon, Kevin E.
;
Hinton, George G.
...
Pediatric Neurology. 4 (1988) 1 - p. 54-57 , 1988
Link:
https://doi.org/10.1016/..
?
14
Genetic control of ganglioside biosynthesis in mice:
Sokoloff, Dina
;
Hechtman, Peter
Biochemical Genetics. 26 (1988) 9-10 - p. 631-644 , 1988
Link:
https://doi.org/10.1007/..
?
15
In Situ Activation of Human Erythrocyte Prolidase: Potentia..:
Hechtman, Peter
;
Richter, Andrea
;
Corman, Natalie
.
Pediatric Research. 24 (1988) 6 - p. 709-712 , 1988
Link:
https://doi.org/10.1203/..
1-15