Glick B - Search Results

1

Antley-Bixler syndrome and esophageal atresia in a patient with trisomy 21.

Feigin E, Udassin R, Seror D, Szold A, Ben Neriah Z, Glick B. Feigin E, et al. Among authors: glick b. Clin Genet. 1995 Jan;47(1):53-5. doi: 10.1111/j.1399-0004.1995.tb03922.x. Clin Genet. 1995. PMID: 7774045

2

Pseudotumor cerebri and coma in vitamin D--dependent rickets.

Alpan G, Glick B, Peleg O, Eyal F. Alpan G, et al. Among authors: glick b. Clin Pediatr (Phila). 1991 Apr;30(4):254-6. doi: 10.1177/000992289103000408. Clin Pediatr (Phila). 1991. PMID: 2025988 No abstract available.

3

Short stature, moderate mental retardation, hyperactivity, facial dysmorphism, skeletal abnormalities, and exaggerated ketosis: a new syndrome.

Boneh A, Glick B, Gutman A, Mogle P. Boneh A, et al. Among authors: glick b. Clin Genet. 1996 Nov;50(5):403-6. doi: 10.1111/j.1399-0004.1996.tb02396.x. Clin Genet. 1996. PMID: 9007332

4

Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.

Zlotogora J, Glick B. Zlotogora J, et al. Among authors: glick b. Am J Med Genet. 1993 Aug 1;47(1):89-90. doi: 10.1002/ajmg.1320470118. Am J Med Genet. 1993. PMID: 8368260 Review.

5

Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome.

Borochowitz Z, Glick B, Blazer S. Borochowitz Z, et al. Among authors: glick b. J Med Genet. 1991 May;28(5):345-8. doi: 10.1136/jmg.28.5.345. J Med Genet. 1991. PMID: 1865475 Free PMC article.

6

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis.

Attali R, Warwar N, Israel A, Gurt I, McNally E, Puckelwartz M, Glick B, Nevo Y, Ben-Neriah Z, Melki J. Attali R, et al. Among authors: glick b. Hum Mol Genet. 2009 Sep 15;18(18):3462-9. doi: 10.1093/hmg/ddp290. Epub 2009 Jun 19. Hum Mol Genet. 2009. PMID: 19542096

7

Down syndrome and attention-deficit/hyperactivity disorder (ADHD).

Ekstein S, Glick B, Weill M, Kay B, Berger I. Ekstein S, et al. Among authors: glick b. J Child Neurol. 2011 Oct;26(10):1290-5. doi: 10.1177/0883073811405201. Epub 2011 May 31. J Child Neurol. 2011. PMID: 21628698

8

Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency.

Elpeleg ON, Havkin S, Barash V, Jakobs C, Glick B, Shalev RS. Elpeleg ON, et al. Among authors: glick b. J Pediatr. 1992 Sep;121(3):407-10. doi: 10.1016/s0022-3476(05)81796-2. J Pediatr. 1992. PMID: 1517917

9

Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.

Lossos A, Elazar N, Lerer I, Schueler-Furman O, Fellig Y, Glick B, Zimmerman BE, Azulay H, Dotan S, Goldberg S, Gomori JM, Ponger P, Newman JP, Marreed H, Steck AJ, Schaeren-Wiemers N, Mor N, Harel M, Geiger T, Eshed-Eisenbach Y, Meiner V, Peles E. Lossos A, et al. Among authors: glick b. Brain. 2015 Sep;138(Pt 9):2521-36. doi: 10.1093/brain/awv204. Epub 2015 Jul 15. Brain. 2015. PMID: 26179919 Free PMC article.

10

Congenital myopathies in Israeli families.

Weiss K, Shapira Y, Glick B, Lerman-Sagie T, Shahar E, Goez H, Kutai M, Nevo Y. Weiss K, et al. Among authors: glick b. J Child Neurol. 2007 Jun;22(6):732-6. doi: 10.1177/0883073807304193. J Child Neurol. 2007. PMID: 17641259

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