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Results: 1-12 |
Results: 12
ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS - A RARE NEUROCUTANEOUS SYNDROME
Authors: CIATTI S DELMONACO M HYDE P BERNSTEIN EF
Citation: S. Ciatti et al., ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS - A RARE NEUROCUTANEOUS SYNDROME, Journal of the American Academy of Dermatology, 38(1), 1998, pp. 102-104
PROLIFERATIVE MYOSITIS - RARE PSEUDOTUMOROUS LESION
Authors: SARTESCHI M CIATTI S SABO C MASSEI P PAOLI R
Citation: M. Sarteschi et al., PROLIFERATIVE MYOSITIS - RARE PSEUDOTUMOROUS LESION, Journal of ultrasound in medicine, 16(11), 1997, pp. 771-773
CLEARANCE OF VASCULAR MALFORMATIONS RESISTANT TO CONVENTIONAL PULSED-DYE LASER TREATMENT WITH THE 595 NM LONG-PULSE TUNABLE DYE-LASER
Authors: KORNBLEUTH S LOWERY J LEE J CIATTI S UITTO J BERNSTEIN EF
Citation: S. Kornbleuth et al., CLEARANCE OF VASCULAR MALFORMATIONS RESISTANT TO CONVENTIONAL PULSED-DYE LASER TREATMENT WITH THE 595 NM LONG-PULSE TUNABLE DYE-LASER, Journal of investigative dermatology, 108(4), 1997, pp. 788-788
THE 585 NM FLASHLAMP-PUMPED PULSED DYE-LASER FOR THE TREATMENT OF TELANGIECTASES IN PATIENTS WITH SCLERODERMA
Authors: CIATTI S VARGA J GREENBAUM SS
Citation: S. Ciatti et al., THE 585 NM FLASHLAMP-PUMPED PULSED DYE-LASER FOR THE TREATMENT OF TELANGIECTASES IN PATIENTS WITH SCLERODERMA, Journal of the American Academy of Dermatology, 35(3), 1996, pp. 487-488
A RECURRENT HOMOZYGOUS NONSENSE MUTATION WITHIN THE LAMA3 GENE AS A CAUSE OF HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA IN PATIENTS OF PAKISTANI ANCESTRY - EVIDENCE FOR A FOUNDER EFFECT
Authors: MCGRATH JA KIVIRIKKO S CIATTI S MOSS C CHRISTIANO AM UITTO J
Citation: Ja. Mcgrath et al., A RECURRENT HOMOZYGOUS NONSENSE MUTATION WITHIN THE LAMA3 GENE AS A CAUSE OF HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA IN PATIENTS OF PAKISTANI ANCESTRY - EVIDENCE FOR A FOUNDER EFFECT, Journal of investigative dermatology, 106(4), 1996, pp. 781-784
A HOMOZYGOUS NONSENSE MUTATION IN THE ALPHA-3 CHAIN GENE OF LAMININ-5(LAMA3) IN LETHAL (HERLITZ) JUNCTIONAL EPIDERMOLYSIS-BULLOSA
Authors: KIVIRIKKO S MCGRATH JA BAUDOIN C ABERDAM D CIATTI S DUNNILL MGS MCMILLAN JR EADY RAJ ORTONNE JP MENEGUZZI G UITTO J CHRISTIANO AM
Citation: S. Kivirikko et al., A HOMOZYGOUS NONSENSE MUTATION IN THE ALPHA-3 CHAIN GENE OF LAMININ-5(LAMA3) IN LETHAL (HERLITZ) JUNCTIONAL EPIDERMOLYSIS-BULLOSA, Human molecular genetics, 4(5), 1995, pp. 959-962
A HOMOZYGOUS NONSENSE MUTATION IN THE ALPHA-3 CHAIN GENE OF LAMININ-5(LAMA3) IN HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA - PRENATAL EXCLUSION IN A FETUS AT RISK
Authors: MCGRATH JA KIVIRIKKO S CIATTI S MOSS C DUNNILL MGS EADY RAJ RODECK CH CHRISTIANO AM UITTO J
Citation: Ja. Mcgrath et al., A HOMOZYGOUS NONSENSE MUTATION IN THE ALPHA-3 CHAIN GENE OF LAMININ-5(LAMA3) IN HERLITZ JUNCTIONAL EPIDERMOLYSIS-BULLOSA - PRENATAL EXCLUSION IN A FETUS AT RISK, Genomics, 29(1), 1995, pp. 282-284
INTERMOLECULAR RECOMBINATION AND USE OF REVERSE COMPLEMENT SPLICE SITES IN THE REGULATED EXPRESSION OF A CHIMERIC TRANSCRIPT IN-VIVO
Authors: DIETZ HC KENDZIOR RJ ABERDAM D BAUDOIN C CIATTI S GUGGINO W MENEGUZZI G UITTO J CHRISTIANO AM
Citation: Hc. Dietz et al., INTERMOLECULAR RECOMBINATION AND USE OF REVERSE COMPLEMENT SPLICE SITES IN THE REGULATED EXPRESSION OF A CHIMERIC TRANSCRIPT IN-VIVO, Pediatric research, 37(4), 1995, pp. 147-147
ORIGINS OF ISOFORM DIVERSITY FROM THE HUMAN LAMA3 GENE - EVIDENCE FORALTERNATIVE SPLICING, INTERMOLECULAR RECOMBINATION, AND CELL-TYPE-SPECIFIC USE OF REVERSE COMPLEMENT SPLICE SITES
Authors: CHRISTIANO AM ABERDAM D CIATTI S BAUDOIN C KENDZIOR RJ ORTONNE JP MENEGUZZI S UITTO J DIETZ HC
Citation: Am. Christiano et al., ORIGINS OF ISOFORM DIVERSITY FROM THE HUMAN LAMA3 GENE - EVIDENCE FORALTERNATIVE SPLICING, INTERMOLECULAR RECOMBINATION, AND CELL-TYPE-SPECIFIC USE OF REVERSE COMPLEMENT SPLICE SITES, Journal of investigative dermatology, 104(4), 1995, pp. 561-561
A HOMOZYGOUS NONSENSE MUTATION WITHIN THE LAMA3 GENE IN LETHAL (HERLITZ) JUNCTIONAL EPIDERMOLYSIS-BULLOSA
Authors: KIVIRIKKO S MCGRATH JA CHRISTIANO AM BAUDOIN C GILES M DUNNILL S CIATTI S MCMILLAN JR ABERDAM D EADY RAJ ORTONNE JP MENEGUZZI G UITTO J
Citation: S. Kivirikko et al., A HOMOZYGOUS NONSENSE MUTATION WITHIN THE LAMA3 GENE IN LETHAL (HERLITZ) JUNCTIONAL EPIDERMOLYSIS-BULLOSA, Journal of investigative dermatology, 104(4), 1995, pp. 569-569
POSITIONAL EFFECTS OF HETEROZYGOUS FRAMESHIFTS IN COL7A1 - SINGLE-BASE DELETIONS WITHIN THE NC-1 AND NC-2 DOMAINS IN THE MITIS FORM OF RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA
Authors: CIATTI S CHRISTIANO AM MCGRATH JA ANHALT G UITTO J
Citation: S. Ciatti et al., POSITIONAL EFFECTS OF HETEROZYGOUS FRAMESHIFTS IN COL7A1 - SINGLE-BASE DELETIONS WITHIN THE NC-1 AND NC-2 DOMAINS IN THE MITIS FORM OF RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA, Journal of investigative dermatology, 104(4), 1995, pp. 598-598
RECURRENT PREMATURE TERMINATION CODON MUTATION IN THE TYPE-VII COLLAGEN GENE (COL7A1) IN 2 FAMILIES WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA IN ITALY
Authors: CIATTI S CHRISTIANO AM PARADISI M MORRICONE A ANGELO C MAZZANTI C CAVALIERI R UITTO J
Citation: S. Ciatti et al., RECURRENT PREMATURE TERMINATION CODON MUTATION IN THE TYPE-VII COLLAGEN GENE (COL7A1) IN 2 FAMILIES WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA IN ITALY, Journal of investigative dermatology, 102(4), 1994, pp. 621-621
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