CHARACTERIZATION OF AN ADENYLATE CYCLASE-LINKED SEROTONIN (5-HT₁) RECEPTOR IN A NEUROBLASTOMA X BRAIN EXPLANT HYBRID CELL LINE (NCB-20)BERRY KRAVIS E; DAWSON G.1983; JOURNAL OF NEUROCHEMISTRY; ISSN 0022-3042; GBR; DA. 1983; VOL. 40; NO 4; PP. 977-985; BIBL. 37 REF.Article

Demonstration of abnormal cyclic AMP production in platelets from patients with fragile X syndromeBERRY-KRAVIS, E; SKLENA, P.American journal of medical genetics. 1993, Vol 45, Num 1, pp 81-87, issn 0148-7299Article

Possible role of gangliosides in regulating an adenylate cyclase-linked 5-hydroxytryptamine (5-HT₁) receptorBERRY-KRAVIS, E; DAWSON, G.Journal of neurochemistry. 1985, Vol 45, Num 6, pp 1739-1747, issn 0022-3042Article

Differential regulation of multiple neuroreceptors in a somatic cell hybrid by inhibitors of glycoprotein processingMCLAWHON, R. W; BERRY-KRAVIS, E; DAWSON, G et al.Biochemical and biophysical research communications (Print). 1986, Vol 134, Num 3, pp 1387-1394, issn 0006-291XArticle

Reduced cyclic AMP production in fragile X syndrome : cytogenetic and molecular correlationsBERRY-KRAVIS, E; HICAR, M; CIURLIONIS, R et al.Pediatric research. 1995, Vol 38, Num 5, pp 638-643, issn 0031-3998Article

X-linked pachygyria and agenesis of the corpus callosum : evidence for an X chromosome lissencephaly locusBERRY-KRAVIS, E; ISRAEL, J.Annals of neurology. 1994, Vol 36, Num 2, pp 229-233, issn 0364-5134Conference Paper

Cyclic AMP metabolism in fragile X syndromeBERRY-KRAVIS, E; HUTTENLOCHER, P. R.Annals of neurology. 1992, Vol 31, Num 1, pp 22-26, issn 0364-5134Article

Two patients with overlapping De Novo duplications of the long arm of chromosome 9, including one case with Di George sequenceLINDGREN, V; ROSINSKY, B; CHIN, J et al.American journal of medical genetics. 1994, Vol 49, Num 1, pp 67-73, issn 0148-7299Article

Heterologous expression of the serotonin 5-HT_1A receptor in neural and non-neural cell linesBANERJEE, P; BERRY-KRAVIS, E; BONAFEDE-CHHABRA, D et al.Biochemical and biophysical research communications (Print). 1993, Vol 192, Num 1, pp 104-110, issn 0006-291XArticle

Neuromodulator-mediated phosphorylation of specific proteins in a neurotumor hybrid cell line (NCB-20)BERRY-KRAVIS, E; KAZMIERCZAK, B. I; DERECHIN, V et al.Journal of neurochemistry. 1988, Vol 50, Num 4, pp 1287-1296, issn 0022-3042Article

Preferential β-hexosaminidase (Hex) A (αβ) formation in the absence of β-Hex B (ββ) due to heterozygous point mutations present in β-Hex β-chain alleles of a motor neuron disease patientPROBAL BANERJEE; BOYERS, M. J; BERRY-KRAVIS, E et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 7, pp 4819-4826, issn 0021-9258Article

FMR1 CGG repeat length predicts motor dysfunction in premutation carriersLEEHEY, M. A; BERRY-KRAVIS, E; GANE, L et al.Neurology. 2008, Vol 70, Num 16, pp 1397-1402, issn 0028-3878, 6 p., 2Article

Aging in individuals with the FMR1 mutationJACQUEMONT, S; FARZIN, F; BERRY-KRAVIS, E et al.American journal on mental retardation. 2004, Vol 109, Num 2, pp 154-164, issn 0895-8017, 11 p.Article

Apolipoprotein E ∈4 allele, AD pathology, and the clinical expression of Alzheimer's diseaseBENNETT, D. A; WILSON, R. S; SCHNEIDER, J. A et al.Neurology. 2003, Vol 60, Num 2, pp 246-252, issn 0028-3878, 7 p.Article

Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeSHEEN, V. L; JANSEN, A; VAID, R. R et al.Neurology. 2005, Vol 64, Num 2, pp 254-262, issn 0028-3878, 9 p.Article

Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS)HALL, D. A; BERRY-KRAVIS, E; JACQUEMONT, S et al.Neurology. 2005, Vol 65, Num 2, pp 299-301, issn 0028-3878, 3 p.Article

The apolipoprotein E ∈4 allele increases the odds of chronic cerebral infection detected at autopsy in older personsSCHNEIDER, J. A; BIENIAS, J. L; WILSON, R. S et al.Stroke (1970). 2005, Vol 36, Num 5, pp 954-959, issn 0039-2499, 6 p.Article

Mosaic trisomy 16 ascertained through amniocentesis : Evaluation of 11 new casesHSU, W.-T; SHCHEPIN, D. A; HAJIANPOUR, M. J et al.American journal of medical genetics. 1998, Vol 80, Num 5, pp 473-480, issn 0148-7299Article

Édition française de la Déclaration officielle de politique clinique de l'American Thoracic Society (ATS) sur le syndrome d'hypoventilation alvéolaire centrale congénitale. Bases génétiques, diagnostic et prise en charge = ATS clinical policy statement: Congenital central hypoventilation syndrome. Genetic basis, diagnosis and managementWEESE-MAYER, D. E; BERRY-KRAVIS, E. M; CECCHERINI, I et al.Revue des maladies respiratoires. 2013, Vol 30, Num 8, pp 706-733, issn 0761-8425, 28 p.Article

Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndromeCHONCHAIYA, W; NGUYEN, D. V; SORENSEN, P et al.Clinical genetics. 2010, Vol 78, Num 1, pp 38-46, issn 0009-9163, 9 p.Article