Found: 49
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Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics.
- Published in:
- Cleft Palate Craniofacial Journal, 2024, v. 61, n. 3, p. 527, doi. 10.1177/10556656221149243
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- Publication type:
- Article
Extensive and Persistent Dermal Melanocytosis in a Male Carrier of Mucopolysaccharidosis Type IIIC (Sanfilippo Syndrome): A Case Report.
- Published in:
- Children, 2023, v. 10, n. 12, p. 1920, doi. 10.3390/children10121920
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- Publication type:
- Article
Newborn Wearing an Ascot Cap.
- Published in:
- Journal of Neonatology, 2023, v. 37, n. 3, p. 273, doi. 10.1177/09732179221142971
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- Publication type:
- Article
Café au lait macules and vitiligo: A conflicting coexistence.
- Published in:
- Pigment International, 2023, v. 10, n. 3, p. 186, doi. 10.4103/pigmentinternational.pigmentinternational_28_22
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- Publication type:
- Article
Fibrous dysplasia and McCune-Albright syndrome: A case report with review of literature on the rehabilitation approach.
- Published in:
- Turkish Journal of Physical Medicine & Rehabilitation (2587-1250), 2023, v. 69, n. 2, p. 252, doi. 10.5606/tftrd.2023.8815
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- Publication type:
- Article
Is neurofibromatosis type 1 diagnosed in every patient who presents with café au lait macules? A single-center experience.
- Published in:
- Marmara Medical Journal, 2023, v. 36, n. 2, p. 192, doi. 10.5472/marumj.1302264
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- Publication type:
- Article
Evaluation of Clinical and Laboratory Features of Patients with Ataxia-Telangiectasia.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2023, v. 21, n. 1, p. 3, doi. 10.21911/aai.006
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- Publication type:
- Article
Multiple hypo- and hyper-pigmentation: An example of twin spotting?
- Published in:
- 2022
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- Publication type:
- Case Study
Plexiform neurofibromatosis of the liver: an extremely rare case.
- Published in:
- Gastroenterology & Hepatology from Bed to Bench, 2022, v. 15, n. 3, p. 282, doi. 10.22037/ghfbb.v15i3.2047
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- Publication type:
- Article
Dermatologic manifestations in paediatric neurofibromatosis type 2: a cross sectional descriptive multicentric study.
- Published in:
- 2022
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- Publication type:
- journal article
Spontaneous Near Fatal Hemorrhage into Neurofibromatosis Type 1 Lesion in the Scalp.
- Published in:
- Oman Medical Journal, 2022, v. 37, n. 3, p. 19, doi. 10.5001/omj.2022.02
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- Publication type:
- Article
Optic nerve glioma in neurofibromatosis: Radiological clues to diagnosis in a young child.
- Published in:
- Journal of Pediatric Neurosciences, 2021, v. 16, n. 3, p. 264, doi. 10.4103/jpn.JPN_189_20
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- Publication type:
- Article
Hyperpigmented spots at fundus examination: a new ocular sign in Neurofibromatosis Type I.
- Published in:
- 2021
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- Publication type:
- journal article
Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?
- Published in:
- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01004-9
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- Publication type:
- Article
Cutaneous Findings in Neurofibromatosis Type 1.
- Published in:
- Cancers, 2021, v. 13, n. 3, p. 463, doi. 10.3390/cancers13030463
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- Publication type:
- Article
Retinal cafe-au-lait macules: A rare retinal finding in a patient with neurofibromatosis type 1.
- Published in:
- 2019
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- Publication type:
- journal article
Fuzzy brown spots on a healthy 3-year-old.
- Published in:
- 2019
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- Publication type:
- Case Study
Brain MRI analysis of six patients with neurofibromatosis type 1.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2019, v. 19, n. 3, p. 205, doi. 10.3969/j.issn.1672-6731.2019.03.011
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- Publication type:
- Article
Mongolian spots combined with halo-like disappearance surrounding café au lait spots.
- Published in:
- 2018
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- Publication type:
- case study
COUNTING THE CALs.
- Published in:
- Community Practitioner, 2018, v. 91, n. 5, p. 25
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- Publication type:
- Article
Picosecond 532-nm neodymium-doped yttrium aluminium garnet laser-a novel and promising modality for the treatment of café-au-lait macules.
- Published in:
- 2018
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- Publication type:
- journal article
Deletion 21pterq22.11: Report of a Patient with Dysmorphic Features, Hypertonia, and Café-au-Lait Macules and Review of the Literature.
- Published in:
- 2018
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- Publication type:
- Case Study
Pigmentation Disorders: Diagnosis and Management.
- Published in:
- 2017
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- Publication type:
- journal article
Response to Laser Treatment of Café au Lait Macules Based on Morphologic Features.
- Published in:
- 2017
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- Publication type:
- journal article
Wood's lamp fluorescence of dihydroxyacetone treated skin.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 11, p. e125, doi. 10.1111/jdv.13401
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- Publication type:
- Article
MCCUNE ALBRIGHT SYNDROME - ASSOCIATION OF FIBROUS DYSPLASIA, CAFÉ-AU-LAIT SKIN SPOTS AND HYPERTHYROIDISM - CASE REPORT.
- Published in:
- 2016
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- Publication type:
- Case Study
Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.
- Published in:
- 2016
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- Publication type:
- journal article
Copy number variants and rasopathies: germline KRAS duplication in a patient with syndrome including pigmentation abnormalities.
- Published in:
- 2016
- By:
- Publication type:
- letter
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study.
- Published in:
- 2016
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- Publication type:
- journal article
Plexiform neurofibromatosis type 1.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Hypomelanosis of Ito associated with cafe-au-lait spot and angiomatous nevi.
- Published in:
- 2015
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- Publication type:
- Case Study
Giant café au lait macule in an infant.
- Published in:
- Indian Journal of Paediatric Dermatology, 2015, v. 16, n. 4, p. 268, doi. 10.4103/2319-7250.165672
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- Publication type:
- Article
Painless Loss of Vision as The First Presentation of Undiagnosed Neurofibromatosis 1 in A Child.
- Published in:
- 2015
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- Publication type:
- Case Study
SEGMENTAL NEUROFIBROMATOSIS 1: A 24-YEAR FOLLOW UP.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
McCune Albright syndrome in association with excessive GH secretion: case report.
- Published in:
- Türk Pediatri Arşivi, 2015, v. 50, n. 2, p. 114, doi. 10.5152/tpa.2015.615
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- Publication type:
- Article
Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence.
- Published in:
- Journal of Pediatric Neurosciences, 2015, v. 10, n. 2, p. 172, doi. 10.4103/1817-1745.159205
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- Publication type:
- Article
Management of common neonatal problems.
- Published in:
- British Journal of Nursing, 2015, v. 24, n. 5, p. 258, doi. 10.12968/bjon.2015.24.5.258
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- Publication type:
- Article
Legius syndrome: case report and review of literature.
- Published in:
- Italian Journal of Pediatrics, 2015, v. 41, n. 1, p. 1, doi. 10.1186/s13052-015-0115-9
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- Publication type:
- Article
Type I Neurofibromatosis Complicated by Large Cell Neuroendocrine Carcinoma of the Lung.
- Published in:
- Turkish Thoracic Journal / Turk Toraks Dergisi, 2014, v. 15, n. 4, p. 168, doi. 10.5152/ttd.2014.4276
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- Publication type:
- Article
Type VIII - Ehlers Danlos Syndrome with café-au-lait macules: A Rare Variant.
- Published in:
- Indian Journal of Dermatology, 2014, v. 59, n. 3, p. 317, doi. 10.4103/0019-5154.131466
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- Publication type:
- Article
Predictive Genetic Testing in Children: Constitutional Mismatch Repair Deficiency Cancer Predisposing Syndrome.
- Published in:
- 2014
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- Publication type:
- Report
Secondary Vascular Alterations in Diffuse and Plexiform Neurofibroma: An Impressive yet Little Known Morphologic Change.
- Published in:
- 2014
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- Publication type:
- Case Study
Association of Piebaldism, Multiple Café-au-lait Macules, and Intertriginous Freckling: Clinical Evidence of a Common Pathway between KIT and Sprouty-Related, Ena/Vasodilator-Stimulated Phosphoprotein Homology-1 Domain Containing Protein 1 (SPRED1)
- Published in:
- Pediatric Dermatology, 2013, v. 30, n. 3, p. 379, doi. 10.1111/j.1525-1470.2012.01858.x
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- Publication type:
- Article
Segmental neurofibromatosis type 1. Differences between the childhood and adult form.
- Published in:
- European Journal of Pediatric Dermatology, 2012, v. 22, n. 4, p. 257
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- Publication type:
- Article
Rumień trwały -- zjawiska patogenetyczne i różnorodność obrazu klinicznego.
- Published in:
- Dermatology Review / Przeglad Dermatologiczny, 2012, v. 99, n. 3, p. 252
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- Publication type:
- Article
A Water-Damaged Home and Health of Occupants: A Case Study.
- Published in:
- 2012
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- Publication type:
- Case Study
Treatment of 153 Japanese patients with Q-switched alexandrite laser.
- Published in:
- 2007
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- Publication type:
- journal article
A 13-year-old girl with neurofibromatosis-1, scoliosis.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Association of urticaria pigmentosa with café-au-lait spots, neurofibromas and neurofibroma-like neoplasms: a mere coincidence?
- Published in:
- 2003
- By:
- Publication type:
- journal article