al-Gazali LI - Search Results

1

Wolcott-Rallison syndrome.

al-Gazali LI, Makia S, Azzam A, Hall CM. al-Gazali LI, et al. Clin Dysmorphol. 1995 Jul;4(3):227-33. Clin Dysmorphol. 1995. PMID: 7551159

2

Birth prevalence and pattern of osteochondrodysplasias in an inbred high risk population.

Al-Gazali LI, Bakir M, Hamid Z, Varady E, Varghes M, Haas D, Bener A, Padmanabhan R, Abdulrrazzaq YM, Dawadu A. Al-Gazali LI, et al. Birth Defects Res A Clin Mol Teratol. 2003 Feb;67(2):125-32. doi: 10.1002/bdra.10009. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 12769508

3

["Body stalk anomaly" (dysplasia umbilico-fetalis) -- an extremely rare malformation].

Langer R, Raupp P, Al-Gazali LI. Langer R, et al. Rofo. 2004 May;176(5):768-9. doi: 10.1055/s-2004-812775. Rofo. 2004. PMID: 15122482 German. No abstract available.

4

Congenital bowing of the long bones associated with camptodactyly, talipes equinovarus and agenesis of the corpus callosum.

Al-Gazali LI, Bakir M, Hamid ZM, Nath R, Haas D. Al-Gazali LI, et al. Clin Dysmorphol. 2000 Apr;9(2):93-7. doi: 10.1097/00019605-200009020-00003. Clin Dysmorphol. 2000. PMID: 10826618

5

Abnormal myelination in peroxisomal isolated dihydroxyacetonephosphate acyltransferase deficiency.

Sztriha LS, Nork MP, Abdulrazzaq YM, al-Gazali LI, Bakalinova DB. Sztriha LS, et al. Pediatr Neurol. 1997 Apr;16(3):232-6. doi: 10.1016/s0887-8994(97)00014-3. Pediatr Neurol. 1997. PMID: 9165515

6

XK aprosencephaly.

al-Gazali LI, Bakalinova D, Bakir M, Nath KN. al-Gazali LI, et al. Clin Dysmorphol. 1998 Apr;7(2):143-7. doi: 10.1097/00019605-199804000-00013. Clin Dysmorphol. 1998. PMID: 9571288 Review.

7

Joubert's syndrome: new cases and review of clinicopathologic correlation.

Sztriha L, Al-Gazali LI, Aithala GR, Nork M. Sztriha L, et al. Pediatr Neurol. 1999 Apr;20(4):274-81. doi: 10.1016/s0887-8994(98)00154-4. Pediatr Neurol. 1999. PMID: 10328276

8

Fibrochondrogenesis: clinical and radiological features.

al-Gazali LI, Bakalinova D, Bakir M, Dawodu A. al-Gazali LI, et al. Clin Dysmorphol. 1997 Apr;6(2):157-63. Clin Dysmorphol. 1997. PMID: 9134297

9

Recurrence of fibrochondrogenesis in a consanguineous family.

al-Gazali LI, Bakir M, Dawodu A, Haas D. al-Gazali LI, et al. Clin Dysmorphol. 1999 Jan;8(1):59-61. Clin Dysmorphol. 1999. PMID: 10327253

10

Recurrence of the severe form of microgastria-limb reduction defect in a consanguineous family.

al-Gazali LI, Bakir M, Dawodu A, Nath R, al-Tatari HM, Gerami M. al-Gazali LI, et al. Clin Dysmorphol. 1999 Oct;8(4):253-8. Clin Dysmorphol. 1999. PMID: 10532173 Review.

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