Bay C - Search Results

1

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.

Muenke M, Gurrieri F, Bay C, Yi DH, Collins AL, Johnson VP, Hennekam RC, Schaefer GB, Weik L, Lubinsky MS, et al. Muenke M, et al. Among authors: bay c. Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8102-6. doi: 10.1073/pnas.91.17.8102. Proc Natl Acad Sci U S A. 1994. PMID: 8058764 Free PMC article.

2

Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.

Bay C, Mauk J, Radcliffe J, Kaplan P. Bay C, et al. Am J Med Genet. 1993 Nov 15;47(7):965-8. doi: 10.1002/ajmg.1320470706. Am J Med Genet. 1993. PMID: 7507294

3

Reversible metabolic myopathy in biotinidase deficiency: its possible role in causing hypotonia.

Bay CA, Berry GT, Glauser TA, Hayward JC, Wolf B, Sladky JT, Kaplan P. Bay CA, et al. J Inherit Metab Dis. 1995;18(6):701-4. doi: 10.1007/BF02436759. J Inherit Metab Dis. 1995. PMID: 8750607

4

Regional variation in brain lactate in Leigh syndrome by localized 1H magnetic resonance spectroscopy.

Detre JA, Wang ZY, Bogdan AR, Gusnard DA, Bay CA, Bingham PM, Zimmerman RA. Detre JA, et al. Among authors: bay ca. Ann Neurol. 1991 Feb;29(2):218-21. doi: 10.1002/ana.410290219. Ann Neurol. 1991. PMID: 2012390

5

Kabuki make-up syndrome associated with an acquired hypogammaglobulinemia and anti-IgA antibodies.

Hostoffer RW, Bay CA, Wagner K, Venglarcik J 3rd, Sahara H, Omair E, Clark HT. Hostoffer RW, et al. Among authors: bay ca. Clin Pediatr (Phila). 1996 May;35(5):273-6. doi: 10.1177/000992289603500509. Clin Pediatr (Phila). 1996. PMID: 8804548 No abstract available.

6

An evaluation of protein requirements in methylmalonic acidaemia.

Ney D, Bay C, Saudubray JM, Kelts DG, Kulovich S, Sweetman L, Nyhan WL. Ney D, et al. Among authors: bay c. J Inherit Metab Dis. 1985;8(3):132-42. doi: 10.1007/BF01819298. J Inherit Metab Dis. 1985. PMID: 3939589

7

Joseph disease and Huntington disease: protein patterns in fibroblasts and brain.

Rosenberg RN, Ivy N, Kirkpatrick J, Bay C, Nyhan WL, Baskin F. Rosenberg RN, et al. Among authors: bay c. Neurology. 1981 Aug;31(8):1003-14. doi: 10.1212/wnl.31.8.1003. Neurology. 1981. PMID: 6455606

8

Neurologic nonmetabolic presentation of propionic acidemia.

Nyhan WL, Bay C, Beyer EW, Mazi M. Nyhan WL, et al. Among authors: bay c. Arch Neurol. 1999 Sep;56(9):1143-7. doi: 10.1001/archneur.56.9.1143. Arch Neurol. 1999. PMID: 10488817

9

Autosomal dominant striatonigral degeneration. A clinical, pathologic, and biochemical study of a new genetic disorder.

Rosenberg RN, Nyhan WL, Bay C, Shore P. Rosenberg RN, et al. Among authors: bay c. Neurology. 1976 Aug;26(8):703-14. doi: 10.1212/wnl.26.8.703. Neurology. 1976. PMID: 945867

10

Joseph disease: protein patterns in fibroblasts and brain.

Rosenberg RN, Thomas L, Baskin F, Kirkpatrick J, Bay C, Nyhan WL. Rosenberg RN, et al. Among authors: bay c. Neurology. 1979 Jul;29(7):917-26. doi: 10.1212/wnl.29.7.917. Neurology. 1979. PMID: 572941

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