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/vufind/Search/Results?lookfor=%22Makrelouf%2C+Mohamed%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Makrelouf%2C+Mohamed%22&type=Person&sort=year
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PubPharm (30)
1
Proposal of a new diagnostic algorithm for adult-onset Still's disease
enthalten in:
Clinical rheumatology
| 2023
von
Daghor-Abbaci, K.
|
Ait Hamadouche, N.
|
Makhloufi, C.
| +21
CommentIn: Clin Rheumatol. 2023 Feb 20;:. - PMID 36802313
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2
Proposal of a new diagnostic algorithm for adult-onset Still’s disease
enthalten in:
Clinical rheumatology
| 2023
von
Daghor-Abbaci, K.
|
Ait Hamadouche, N.
|
Makhloufi, C.
| +21
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3
Validation of the neutrophil-to-lymphocyte ratio as a new simple biomarker of adult onset Still's disease : A STROBE-Compliant prospective observational study
enthalten in:
Medicine
| 2022
von
Daghor Abbaci, K.
|
Ait Hamadouche, N.
|
Otmani, F.
| +21
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4
Reconsidering vitamin D optimal values based on parathyroid hormone levels in a North Algerian cohort : stratification by gender and season
enthalten in:
Archives of osteoporosis
| 2022
von
Bennouar, S.
|
Bachir Cherif, A.
|
Makrelouf, M.
| +3
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5
Reconsidering vitamin D optimal values based on parathyroid hormone levels in a North Algerian cohort: stratification by gender and season
enthalten in:
Archives of osteoporosis
| 2022
von
Bennouar, S.
|
Bachir Cherif, A.
|
Makrelouf, M.
| +3
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6
Reconsidering vitamin D optimal values based on parathyroid hormone levels in a North Algerian cohort: stratification by gender and season
enthalten in:
Archives of osteoporosis
| 2022
von
Bennouar, S.
|
Bachir Cherif, A.
|
Makrelouf, M.
| +3
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7
IL36RN Mutations Affect Protein Expression and Function : A Basis for Genotype-Phenotype Correlation in Pustular Diseases
enthalten in:
The Journal of investigative dermatology
| 2016
von
Tauber, M.
|
Bal, E.
|
Pei, X.
| +17
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8
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family
enthalten in:
International journal of pediatric otorhinolaryngology
| 2016
von
Behlouli, A.
|
Bonnet, C.
|
Abdi, S.
| +8
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9
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
enthalten in:
PloS one
| 2016
von
Abdi, S.
|
Bahloul, A.
|
Behlouli, A.
| +13
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10
IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases
enthalten in:
The journal of investigative dermatology
| 2016
von
Tauber, M.
|
Bal, E.
|
Pei, X.
| +17
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Medienart
30
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Zeitschriftentitel
4
American journal of human genetics
3
Archives of osteoporosis
3
European journal of medical genetics
2
Archives of medical research
2
Clinical rheumatology
2
International journal of pediatric otorhinolary...
2
Orphanet journal of rare diseases
2
Revue française des laboratoires
2
The journal of investigative dermatology
1
Annales de biologie clinique
1
EMBO molecular medicine
1
Journal of interferon & cytokine research
1
Journal of interferon & cytokine research : the...
1
Medicine
1
PloS one
1
The Journal of investigative dermatology
1
The Lancet. Neurology
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Thema
15
Journal Article
6
Research Support, Non-U.S. Gov't
3
25-Hydroxyvitamin D
3
Inverse non-linear regression
3
Optimal value
3
Parathyroid hormone
2
Adult-onset Still’s disease
2
CDHR15, human
2
Cadherin Related Proteins
2
Cadherins
2
Classification criteria
2
Congenital deafness
2
DNA Primers
2
Diagnostic algorithm
2
Glycosylated ferritin
2
Multicenter Study
2
Neutrophil-to-lymphocyte ratio
2
Review
2
Typical rash
1
0R0008Q3JB
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2020-
14
2010-2019
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2000-2009
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